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Sample records for porous carbon nanofibers

  1. Facile synthesis of carbon nanofibers-bridged porous carbon nanosheets for high-performance supercapacitors

    NASA Astrophysics Data System (ADS)

    Jiang, Yuting; Yan, Jun; Wu, Xiaoliang; Shan, Dandan; Zhou, Qihang; Jiang, Lili; Yang, Deren; Fan, Zhuangjun

    2016-03-01

    A facile and one-step method is demonstrated to prepare carbon nanofibers (CNFs)-bridged porous carbon nanosheets (PCNs) through carbonization of the mixture of bacterial cellulose and potassium citrate. The CNFs bridge PCNs to form integrated porous carbon architecture with high specific surface area of 1037 m2 g-1, much higher than those of pure PCNs (381 m2 g-1) and CNFs (510 m2 g-1). As a consequence, the PCN/CNF composite displays high specific capacitance of 261 F g-1, excellent rate capability and outstanding cycling stability (97.6% of capacitance retention after 10000 cycles). Moreover, the assembled symmetric supercapacitor with PCN/CNF electrodes delivers an ultrahigh energy density of 20.4 Wh kg-1 and outstanding cycling life (94.8% capacitance retention after 10000 cycles) in an aqueous electrolyte.

  2. Synthesis and photocatalytic property of porous metal oxides nanowires based on carbon nanofiber template

    NASA Astrophysics Data System (ADS)

    Fan, Weiqiang; Li, Meng; Xu, Jinfu; Bai, Hongye; Zhang, Rongxian; Chen, Chao

    2015-11-01

    A series of porous metal oxides nanowires (Fe2O3, Co3O4, NiO and CuO) have been successfully synthesized, where commercial carbon nanofibers were used as the template. The obtained samples were systematically characterized by scanning electron microscopy (SEM), X-ray diffraction (XRD), UV-Vis diffuse reflectance (UV-Vis DR) spectra and transmission electron microscope (TEM). According to the photodegradation data, the porous metal oxides nanowires exhibit significantly photocatalytic activity for degrading tetracycline (TC). Furthermore, the porous Fe2O3 nanowires show the best photocatalytic performance among all the samples.

  3. Polyaniline-coated freestanding porous carbon nanofibers as efficient hybrid electrodes for supercapacitors

    NASA Astrophysics Data System (ADS)

    Tran, Chau; Singhal, Richa; Lawrence, Daniel; Kalra, Vibha

    2015-10-01

    Three-dimensional, free-standing, hybrid supercapacitor electrodes combining polyaniline (PANI) and porous carbon nanofibers (P-CNFs) were fabricated with the aim to integrate the benefits of both electric double layer capacitors (high power, cyclability) and pseudocapacitors (high energy density). A systematic investigation of three different electropolymerization techniques, namely, potentiodynamic, potentiostatic, and galvanostatic, for electrodeposition of PANI on freestanding carbon nanofiber mats was conducted. It was found that the galvanostatic method, where the current density is kept constant and can be easily controlled facilitates conformal and uniform coating of PANI on three-dimensional carbon nanofiber substrates. The electrochemical tests indicated that the PANI-coated P-CNFs exhibit excellent specific capacitance of 366 F g-1 (vs. 140 F g-1 for uncoated porous carbon nanofibers), 140 F cm-3 volumetric capacitance, and up to 2.3 F cm-2 areal capacitance at 100 mV s-1 scan rate. Such excellent performance is attributed to a thin and conformal coating of PANI achieved using the galvanostatic electrodeposition technique, which not only provides pseudocapacitance with high rate capability, but also retains the double-layer capacitance of the underlying P-CNFs.

  4. Carbon-Encapsulated Hollow Porous Vanadium-Oxide Nanofibers for Improved Lithium Storage Properties.

    PubMed

    An, Geon-Hyoung; Lee, Do-Young; Ahn, Hyo-Jin

    2016-08-01

    Carbon-encapsulated hollow porous vanadium-oxide (C/HPV2O5) nanofibers have been fabricated using electrospinning and postcalcination. By optimized postcalcination of vanadium-nitride and carbon-nanofiber composites at 400 °C for 30 min, we synthesized a unique architecture electrode with interior void spaces and well-defined pores as well as a uniform carbon layer on the V2O5 nanofiber surface. The optimized C/HPV2O5 electrode postcalcined at 400 °C for 30 min showed improved lithium storage properties with high specific discharge capacities, excellent cycling durability (241 mA h g(-1) at 100 cycles), and improved high-rate performance (155 mA h g(-1) at 1000 mA g(-1)), which is the highest performance in comparison with previously reported V2O5-based cathode materials. The improved electrochemical feature is due to the attractive properties of the carbon-encapsulated hollow porous structure: (I) excellent cycling durability with high specific capacity relative to the adoption of carbon encapsulation as a physical buffer layer and the effective accommodation of volume changes due to the hollow porous structure, (II) improved high-rate performance because of a shorter Li-ion diffusion pathway resulting from interior void spaces and well-defined pores at the surface. This unique electrode structure can potentially provide new cathode materials for high-performance lithium-ion batteries. PMID:27404906

  5. Porous Carbon Nanofibers from Electrospun Biomass Tar/Polyacrylonitrile/Silver Hybrids as Antimicrobial Materials.

    PubMed

    Song, Kunlin; Wu, Qinglin; Zhang, Zhen; Ren, Suxia; Lei, Tingzhou; Negulescu, Ioan I; Zhang, Quanguo

    2015-07-15

    A novel route to fabricate low-cost porous carbon nanofibers (CNFs) using biomass tar, polyacrylonitrile (PAN), and silver nanoparticles has been demonstrated through electrospinning and subsequent stabilization and carbonization processes. The continuous electrospun nanofibers had average diameters ranging from 392 to 903 nm. The addition of biomass tar resulted in increased fiber diameters, reduced thermal stabilities, and slowed cyclization reactions of PAN in the as-spun nanofibers. After stabilization and carbonization, the resultant CNFs showed more uniformly sized and reduced average diameters (226-507 nm) compared to as-spun nanofibers. The CNFs exhibited high specific surface area (>400 m(2)/g) and microporosity, attributed to the combined effects of phase separations of the tar and PAN and thermal decompositions of tar components. These pore characteristics increased the exposures and contacts of silver nanoparticles to the bacteria including Gram-positive Staphylococcus aureus and Gram-negative Escherichia coli, leading to excellent antimicrobial performances of as-spun nanofibers and CNFs. A new strategy is thus provided for utilizing biomass tar as a low-cost precursor to prepare functional CNFs and reduce environmental pollutions associated with direct disposal of tar as an industrial waste. PMID:26110209

  6. Porous block nanofiber composite filters

    DOEpatents

    Ginley, David S.; Curtis, Calvin J.; Miedaner, Alexander; Weiss, Alan J.; Paddock, Arnold

    2016-08-09

    Porous block nano-fiber composite (110), a filtration system (10) and methods of using the same are disclosed. An exemplary porous block nano-fiber composite (110) includes a porous block (100) having one or more pores (200). The porous block nano-fiber composite (110) also includes a plurality of inorganic nano-fibers (211) formed within at least one of the pores (200).

  7. Electrospun carbon nanofibers reinforced 3D porous carbon polyhedra network derived from metal-organic frameworks for capacitive deionization

    PubMed Central

    Liu, Yong; Ma, Jiaqi; Lu, Ting; Pan, Likun

    2016-01-01

    Carbon nanofibers reinforced 3D porous carbon polyhedra network (e-CNF-PCP) was prepared through electrospinning and subsequent thermal treatment. The morphology, structure and electrochemical performance of the e-CNF-PCP were characterized using scanning electron microscopy, Raman spectra, nitrogen adsorption-desorption, cyclic voltammetry and electrochemical impedance spectroscopy, and their electrosorption performance in NaCl solution was studied. The results show that the e-CNF-PCP exhibits a high electrosorption capacity of 16.98 mg g−1 at 1.2 V in 500 mg l−1 NaCl solution, which shows great improvement compared with those of electrospun carbon nanofibers and porous carbon polyhedra. The e-CNF-PCP should be a very promising candidate as electrode material for CDI applications. PMID:27608826

  8. Electrospun carbon nanofibers reinforced 3D porous carbon polyhedra network derived from metal-organic frameworks for capacitive deionization.

    PubMed

    Liu, Yong; Ma, Jiaqi; Lu, Ting; Pan, Likun

    2016-01-01

    Carbon nanofibers reinforced 3D porous carbon polyhedra network (e-CNF-PCP) was prepared through electrospinning and subsequent thermal treatment. The morphology, structure and electrochemical performance of the e-CNF-PCP were characterized using scanning electron microscopy, Raman spectra, nitrogen adsorption-desorption, cyclic voltammetry and electrochemical impedance spectroscopy, and their electrosorption performance in NaCl solution was studied. The results show that the e-CNF-PCP exhibits a high electrosorption capacity of 16.98 mg g(-1) at 1.2 V in 500 mg l(-1) NaCl solution, which shows great improvement compared with those of electrospun carbon nanofibers and porous carbon polyhedra. The e-CNF-PCP should be a very promising candidate as electrode material for CDI applications. PMID:27608826

  9. Controlling SEI Formation on SnSb-Porous Carbon Nanofibers for Improved Na Ion Storage

    SciTech Connect

    Ji, Liwen; Gu, Meng; Shao, Yuyan; Li, Xiaolin; Engelhard, Mark H.; Arey, Bruce W.; Wang, Wei; Nie, Zimin; Xiao, Jie; Wang, Chong M.; Zhang, Jiguang; Liu, Jun

    2014-05-14

    Porous carbon nanofiber (CNF)-supported tin-antimony (SnSb) alloys is synthesized and applied as sodium ion battery anode. The chemistry and morphology of the solid electrolyte interphase (SEI) film and its correlation with the electrode performance are studied. The addition of fluoroethylene carbonate (FEC) in electrolyte significantly reduces electrolyte decomposition and creates a very thin and uniform SEI layer on the cycled electrode surface which could promote the kinetics of Na-ion migration/transportation, leading to excellent electrochemical performance.

  10. Hollow porous carbon nitride immobilized on carbonized nanofibers for highly efficient visible light photocatalytic removal of NO.

    PubMed

    Wu, Hongxin; Chen, Dongyun; Li, Najun; Xu, Qingfeng; Li, Hua; He, Jinghui; Lu, Jianmei

    2016-06-01

    With the deterioration of air quality, great efforts were devoted to designing various photocatalysts for effective removal of NOx in air. However, the present photocatalysts have a fatal problem of low photocatalytic efficiency. In this work, a hollow porous carbon nitride nanosphere coupled with reduced graphene oxide (HCNS/rGO) was exploited as a visible-light photocatalyst to remove nitrogen monoxide in air at a low concentration (600 ppb level) under irradiation of an energy saving lamp. HCNS/rGO showed a NO removal ratio of 64%, which was superior to that of most other visible-light photocatalysts. The excellent photocatalytic ability of HCNS/rGO originates from the hollow porous morphology of HCNS and the grafted rGO on the surface. HCNS/rGO was immobilized on porous carbonized polymer nanofibers to obtain a photocatalytic membrane without affecting photocatalytic efficiency. Furthermore, the membrane showed excellent photochemical stability and recyclability. PMID:27245319

  11. Hollow porous carbon nitride immobilized on carbonized nanofibers for highly efficient visible light photocatalytic removal of NO

    NASA Astrophysics Data System (ADS)

    Wu, Hongxin; Chen, Dongyun; Li, Najun; Xu, Qingfeng; Li, Hua; He, Jinghui; Lu, Jianmei

    2016-06-01

    With the deterioration of air quality, great efforts were devoted to designing various photocatalysts for effective removal of NOx in air. However, the present photocatalysts have a fatal problem of low photocatalytic efficiency. In this work, a hollow porous carbon nitride nanosphere coupled with reduced graphene oxide (HCNS/rGO) was exploited as a visible-light photocatalyst to remove nitrogen monoxide in air at a low concentration (600 ppb level) under irradiation of an energy saving lamp. HCNS/rGO showed a NO removal ratio of 64%, which was superior to that of most other visible-light photocatalysts. The excellent photocatalytic ability of HCNS/rGO originates from the hollow porous morphology of HCNS and the grafted rGO on the surface. HCNS/rGO was immobilized on porous carbonized polymer nanofibers to obtain a photocatalytic membrane without affecting photocatalytic efficiency. Furthermore, the membrane showed excellent photochemical stability and recyclability.With the deterioration of air quality, great efforts were devoted to designing various photocatalysts for effective removal of NOx in air. However, the present photocatalysts have a fatal problem of low photocatalytic efficiency. In this work, a hollow porous carbon nitride nanosphere coupled with reduced graphene oxide (HCNS/rGO) was exploited as a visible-light photocatalyst to remove nitrogen monoxide in air at a low concentration (600 ppb level) under irradiation of an energy saving lamp. HCNS/rGO showed a NO removal ratio of 64%, which was superior to that of most other visible-light photocatalysts. The excellent photocatalytic ability of HCNS/rGO originates from the hollow porous morphology of HCNS and the grafted rGO on the surface. HCNS/rGO was immobilized on porous carbonized polymer nanofibers to obtain a photocatalytic membrane without affecting photocatalytic efficiency. Furthermore, the membrane showed excellent photochemical stability and recyclability. Electronic supplementary information

  12. Tin nanoparticle-loaded porous carbon nanofiber composite anodes for high current lithium-ion batteries

    NASA Astrophysics Data System (ADS)

    Shen, Zhen; Hu, Yi; Chen, Yanli; Zhang, Xiangwu; Wang, Kehao; Chen, Renzhong

    2015-03-01

    Metallic Sn is a promising high-capacity anode material for use in lithium-ion batteries (LIBs), but its huge volume variation during lithium ion insertion/extraction typically results in poor cycling stability. To address this, we demonstrate the fabrication of Sn nanoparticle-loaded porous carbon nanofiber (Sn-PCNF) composites via the electrospinning of Sn(II) acetate/mineral oil/polyacrylonitrile precursors in N,N-dimethylformamide solvent and their subsequent carbonization at 700 °C under an argon atmosphere. This is shown to result in an even distribution of pores on the surface of the nanofibers, allowing the Sn-PCNF composite to be used directly as an anode in lithium-ion batteries without the need to add non-active materials such as polymer binders or electrical conductors. With a discharge capacity of around 774 mA h g-1 achieved at a high current of 0.8 A g-1 over 200 cycles, this material clearly has a high rate capability and excellent cyclic stability, and thanks to its unique structure and properties, is an excellent candidate for use as an anode material in high-current rechargeable lithium-ion batteries.

  13. Free-standing porous carbon nanofiber/ultrathin graphite hybrid for flexible solid-state supercapacitors.

    PubMed

    Qin, Kaiqiang; Kang, Jianli; Li, Jiajun; Shi, Chunsheng; Li, Yuxiang; Qiao, Zhijun; Zhao, Naiqin

    2015-01-27

    A micrometer-thin solid-state supercapacitor (SC) was assembled using two pieces of porous carbon nanofibers/ultrathin graphite (pCNFs/G) hybrid films, which were one-step synthesized by chemical vapor deposition using copper foil supported Co catalyst. The continuously ultrathin graphite sheet (∼ 25 nm) is mechanically compliant to support the pCNFs even after etching the copper foil and thus can work as both current collector and support directly with nearly ignorable fraction in a SC stack. The pCNFs are seamlessly grown on the graphite sheet with an ohmic contact between the pCNFs and the graphite sheet. Thus, the accumulated electrons/ions can duly transport from the pCNFs to graphite (current collector), which results in a high rate performance. The maximum energy density and power density based on the whole device are up to 2.4 mWh cm(-3) and 23 W cm(-3), which are even orders higher than those of the most reported electric double-layer capacitors and pseudocapacitors. Moreover, the specific capacitance of the device has 96% retention after 5000 cycles and is nearly constant at various curvatures, suggesting its wide application potential in powering wearable/miniaturized electronics. PMID:25567451

  14. Highly Flexible Freestanding Porous Carbon Nanofibers for Electrodes Materials of High-Performance All-Carbon Supercapacitors.

    PubMed

    Liu, Ying; Zhou, Jinyuan; Chen, Lulu; Zhang, Peng; Fu, Wenbin; Zhao, Hao; Ma, Yufang; Pan, Xiaojun; Zhang, Zhenxing; Han, Weihua; Xie, Erqing

    2015-10-28

    Highly flexible porous carbon nanofibers (P-CNFs) were fabricated by electrospining technique combining with metal ion-assistant acid corrosion process. The resultant fibers display high conductivity and outstanding mechanical flexibility, whereas little change in their resistance can be observed under repeatedly bending, even to 180°. Further results indicate that the improved flexibility of P-CNFs can be due to the high graphitization degree caused by Co ions. In view of electrode materials for high-performance supercapacitors, this type of porous nanostructure and high graphitization degree could synergistically facilitate the electrolyte ion diffusion and electron transportation. In the three electrodes testing system, the resultant P-CNFs electrodes can exhibit a specific capacitance of 104.5 F g(-1) (0.2 A g(-1)), high rate capability (remain 56.5% at 10 A g(-1)), and capacitance retention of ∼94% after 2000 cycles. Furthermore, the assembled symmetric supercapacitors showed a high flexibility and can deliver an energy density of 3.22 Wh kg(-1) at power density of 600 W kg(-1). This work might open a way to improve the mechanical properties of carbon fibers and suggests that this type of freestanding P-CNFs be used as effective electrode materials for flexible all-carbon supercapacitors. PMID:26449440

  15. Free-standing porous carbon nanofibers-sulfur composite for flexible Li-S battery cathode

    NASA Astrophysics Data System (ADS)

    Zeng, Linchao; Pan, Fusen; Li, Weihan; Jiang, Yu; Zhong, Xiongwu; Yu, Yan

    2014-07-01

    Flexible and free-standing sulphur/(PCNFs-CNT) composite (S@PCNFs-CNT) electrode was successfully prepared by infiltrating sulfur into microporous carbon nanofibers-carbon nanotube (PCNFs-CNT) composite. When used as a cathode material for Li-S batteries, the S@PCNFs-CNT exhibits much better cycle performance and rate performance compared to CNT-free S@PCNFs. It delivers a reversible capacity of 637 mA h g-1 after 100 cycles at 50 mA g-1 and a rate capability of 437 mA h g-1 at 1 A g-1. The improved electrochemical performance is attributed to synergistic effect of the 3D interconnected structure, the additive of CNT, and the uniform distribution of micropores (<2 nm) in the PCNFs-CNT matrix. Our results indicate the potential suitability of PCNFs-CNT for efficient, free-standing, and high-performance batteries.

  16. Free-standing porous carbon nanofibers-sulfur composite for flexible Li-S battery cathode.

    PubMed

    Zeng, Linchao; Pan, Fusen; Li, Weihan; Jiang, Yu; Zhong, Xiongwu; Yu, Yan

    2014-08-21

    Flexible and free-standing sulphur/(PCNFs-CNT) composite (S@PCNFs-CNT) electrode was successfully prepared by infiltrating sulfur into microporous carbon nanofibers-carbon nanotube (PCNFs-CNT) composite. When used as a cathode material for Li-S batteries, the S@PCNFs-CNT exhibits much better cycle performance and rate performance compared to CNT-free S@PCNFs. It delivers a reversible capacity of 637 mA h g(-1) after 100 cycles at 50 mA g(-1) and a rate capability of 437 mA h g(-1) at 1 A g(-1). The improved electrochemical performance is attributed to synergistic effect of the 3D interconnected structure, the additive of CNT, and the uniform distribution of micropores (<2 nm) in the PCNFs-CNT matrix. Our results indicate the potential suitability of PCNFs-CNT for efficient, free-standing, and high-performance batteries. PMID:25008943

  17. Carbon-Confined SnO2-Electrodeposited Porous Carbon Nanofiber Composite as High-Capacity Sodium-Ion Battery Anode Material.

    PubMed

    Dirican, Mahmut; Lu, Yao; Ge, Yeqian; Yildiz, Ozkan; Zhang, Xiangwu

    2015-08-26

    Sodium resources are inexpensive and abundant, and hence, sodium-ion batteries are promising alternative to lithium-ion batteries. However, lower energy density and poor cycling stability of current sodium-ion batteries prevent their practical implementation for future smart power grid and stationary storage applications. Tin oxides (SnO2) can be potentially used as a high-capacity anode material for future sodium-ion batteries, and they have the advantages of high sodium storage capacity, high abundance, and low toxicity. However, SnO2-based anodes still cannot be used in practical sodium-ion batteries because they experience large volume changes during repetitive charge and discharge cycles. Such large volume changes lead to severe pulverization of the active material and loss of electrical contact between the SnO2 and carbon conductor, which in turn result in rapid capacity loss during cycling. Here, we introduce a new amorphous carbon-coated SnO2-electrodeposited porous carbon nanofiber (PCNF@SnO2@C) composite that not only has high sodium storage capability, but also maintains its structural integrity while ongoing repetitive cycles. Electrochemical results revealed that this SnO2-containing nanofiber composite anode had excellent electrochemical performance including high-capacity (374 mAh g(-1)), good capacity retention (82.7%), and large Coulombic efficiency (98.9% after 100th cycle). PMID:26252051

  18. Porous Core-Shell Fe3C Embedded N-doped Carbon Nanofibers as an Effective Electrocatalysts for Oxygen Reduction Reaction.

    PubMed

    Ren, Guangyuan; Lu, Xianyong; Li, Yunan; Zhu, Ying; Dai, Liming; Jiang, Lei

    2016-02-17

    The development of nonprecious-metal-based electrocatalysts with high oxygen reduction reaction (ORR) activity, low cost, and good durability in both alkaline and acidic media is very important for application of full cells. Herein, we developed a facile and economical strategy to obtain porous core-shell Fe3C embedded nitrogen-doped carbon nanofibers (Fe3C@NCNF-X, where X denotes pyrolysis temperature) by electrospinning of polyvinylidene fluoride (PVDF) and FeCl3 mixture, chemical vapor phase polymerization of pyrrole, and followed by pyrolysis of composite nanofibers at high temperatures. Note that the FeCl3 and polypyrrole acts as precursor for Fe3C core and N-doped carbon shell, respectively. Moreover, PVDF not only plays a role as carbon resources, but also provides porous structures due to hydrogen fluoride exposure originated from thermal decomposition of PVDF. The resultant Fe3C@NCNF-X catalysts, particularly Fe3C@NCNF-900, showed efficient electrocatalytic performance for ORR in both alkaline and acidic solutions, which are attributed to the synergistic effect between Fe3C and N-doped carbon as catalytic active sites, and carbon shell protects Fe3C from leaching out. In addition, the Fe3C@NCNF-X catalyst displayed a better long-term stability, free from methanol crossover and CO-poisoning effects than those of Pt/C, which is of great significance for the design and development of advanced electrocatalysts based on nonprecious metals. PMID:26808226

  19. Synthesis of SnO2 versus Sn crystals within N-doped porous carbon nanofibers via electrospinning towards high-performance lithium ion batteries.

    PubMed

    Wang, Hongkang; Lu, Xuan; Li, Longchao; Li, Beibei; Cao, Daxian; Wu, Qizhen; Li, Zhihui; Yang, Guang; Guo, Baolin; Niu, Chunming

    2016-04-14

    The design of tin-based anode materials (SnO2 or Sn) has become a major concern for lithium ion batteries (LIBs) owing to their different inherent characteristics. Herein, particulate SnO2 or Sn crystals coupled with porous N-doped carbon nanofibers (denoted as SnO2/PCNFs and Sn/PCNFs, respectively) are fabricated via the electrospinning method. The electrochemical behaviors of both SnO2/PCNFs and Sn/PCNFs are systematically investigated as anodes for LIBs. When coupled with porous carbon nanofibers, both SnO2 nanoparticles and Sn micro/nanoparticles display superior cycling and rate performances. SnO2/PCNFs and Sn/PCNFs deliver discharge capacities of 998 and 710 mA h g(-1) after 140 cycles (at 100, 200, 500 and 1000 mA g(-1) each for 10 cycles and then 100 cycles at 100 mA g(-1)), respectively. However, the Sn/PCNF electrodes show better cycling stability at higher current densities, delivering higher discharge capacities of 700 and 550 mA h g(-1) than that of SnO2/PCNFs (685 and 424 mA h g(-1)) after 160 cycles at 200 and 500 mA g(-1), respectively. The different superior electrochemical performance is attributed to the introduction of porous N-doped carbon nanofibers and their self-constructed networks, which, on the one hand, greatly decrease the charge-transfer resistance due to the high conductivity of N-doped carbon fibers; on the other hand, the porous carbon nanofibers with numerous voids and flexible one-dimensional (1D) structures efficiently alleviate the volume changes of SnO2 and Sn during the Li-Sn alloying-dealloying processes. Moreover, the discussion of the electrochemical behaviors of SnO2vs. Sn would provide new insights into the design of tin-based anode materials for practical applications, and the current strategy demonstrates great potential in the rational design of metallic tin-based anode materials. PMID:26984273

  20. Direct growth of carbon nanofibers to generate a 3D porous platform on a metal contact to enable an oxygen reduction reaction.

    PubMed

    Pan, David; Ombaba, Matthew; Zhou, Zhi-You; Liu, Yang; Chen, Shaowei; Lu, Jennifer

    2012-12-21

    For carbon nanotube-based electronics to achieve their full performance potential, it is imperative to minimize the contact resistance between macroscale metal contacts and the carbon nanotube (CNT) nanoelectrodes. We have developed a three-dimensional electrode platform that consists of carbon nanofibers (CNFs) that are directly grown on a metal contact, such as copper (Cu). Carbon nanofiber morphology can be tailored by adjusting the annealing time of a thin electrochemically deposited nickel catalyst layer on copper. We demonstrate that increasing the annealing time increases the amount of copper infused into the nickel catalyst layer. This reduces the carbon deposition rate, and consequently a more well-defined CNF 3D architecture can be fabricated. This direct growth of CNFs on a Cu substrate yields an excellent electron transfer pathway, with contact resistance between CNFs and Cu being comparable to that of a Cu-Cu interface. Furthermore, the excellent bonding strength between CNFs and Cu can be maintained over prolonged periods of ultrasonication. The porous 3D platform affixed with intertwined CNFs allows facile surface functionalization. Using a simple solution soaking procedure, the CNF surface has been successfully functionalized with iron(II) phthalocyanine (FePc). FePc functionalized CNFs exhibit excellent oxygen reduction capability, equivalent to platinum-carbon electrodes. This result demonstrates the technological promise of this new 3D electrode platform that can be exploited in other applications that include sensing, battery, and supercapacitors. PMID:23171171

  1. Synthesis of SnO2versus Sn crystals within N-doped porous carbon nanofibers via electrospinning towards high-performance lithium ion batteries

    NASA Astrophysics Data System (ADS)

    Wang, Hongkang; Lu, Xuan; Li, Longchao; Li, Beibei; Cao, Daxian; Wu, Qizhen; Li, Zhihui; Yang, Guang; Guo, Baolin; Niu, Chunming

    2016-03-01

    The design of tin-based anode materials (SnO2 or Sn) has become a major concern for lithium ion batteries (LIBs) owing to their different inherent characteristics. Herein, particulate SnO2 or Sn crystals coupled with porous N-doped carbon nanofibers (denoted as SnO2/PCNFs and Sn/PCNFs, respectively) are fabricated via the electrospinning method. The electrochemical behaviors of both SnO2/PCNFs and Sn/PCNFs are systematically investigated as anodes for LIBs. When coupled with porous carbon nanofibers, both SnO2 nanoparticles and Sn micro/nanoparticles display superior cycling and rate performances. SnO2/PCNFs and Sn/PCNFs deliver discharge capacities of 998 and 710 mA h g-1 after 140 cycles (at 100, 200, 500 and 1000 mA g-1 each for 10 cycles and then 100 cycles at 100 mA g-1), respectively. However, the Sn/PCNF electrodes show better cycling stability at higher current densities, delivering higher discharge capacities of 700 and 550 mA h g-1 than that of SnO2/PCNFs (685 and 424 mA h g-1) after 160 cycles at 200 and 500 mA g-1, respectively. The different superior electrochemical performance is attributed to the introduction of porous N-doped carbon nanofibers and their self-constructed networks, which, on the one hand, greatly decrease the charge-transfer resistance due to the high conductivity of N-doped carbon fibers; on the other hand, the porous carbon nanofibers with numerous voids and flexible one-dimensional (1D) structures efficiently alleviate the volume changes of SnO2 and Sn during the Li-Sn alloying-dealloying processes. Moreover, the discussion of the electrochemical behaviors of SnO2vs. Sn would provide new insights into the design of tin-based anode materials for practical applications, and the current strategy demonstrates great potential in the rational design of metallic tin-based anode materials.The design of tin-based anode materials (SnO2 or Sn) has become a major concern for lithium ion batteries (LIBs) owing to their different inherent

  2. In situ fabrication of three-dimensional nitrogen and boron co-doped porous carbon nanofibers for high performance lithium-ion batteries

    NASA Astrophysics Data System (ADS)

    Zhang, Lijun; Xia, Guanglin; Guo, Zaiping; Sun, Dalin; Li, Xingguo; Yu, Xuebin

    2016-08-01

    This paper reports the fabrication of three-dimensional porous carbon nanofibers network with high doping level of nitrogen (N, 5.17 at.%) and boron (B, 6.87 at.%) through a general electrospinning strategy followed by a calcination process. The employed ammonia borane (NH3BH3, denote as AB) not only functions as a porogen reagent to generate porous structures but also as the heteroatoms source to induce N and B co-doping. Such highly unique nanoarchitectures offer remarkably improved Li storage performance including high reversible capacity (∼910 mAh g-1 at a current density of 100 mA g-1) with good cycling and rate performances.

  3. Direct synthesis of novel vanadium oxide embedded porous carbon nanofiber decorated with iron nanoparticles as a low-cost and highly efficient visible-light-driven photocatalyst.

    PubMed

    Taha, Ahmed Aboueloyoun; Hriez, Amir A; Wu, Yi-nan; Wang, Hongtao; Li, Fengting

    2014-03-01

    Template-free porous carbon nanofibers embedded by vanadium oxide and decorated with iron nanoparticles (Fe@V-CNF) were prepared in a time and cost-saving manner by combining electrospinning and heat treatment processes. Cost-saving ammonium metavanadate was used as a semiconductor precursor of vanadium oxide (VOx) as well as porogen. The generated pores in the carbon nanofiber (CNFs) matrix formed pathways between the embedded VOx and the surface of CNFs and Fe NPs, thus, facilitate photo-generated electron transfer. The characterization results revealed that Fe@V-CNF comprised graphitic fibers with well-dispersed distribution of nanosized Fe NPs (~7 nm) along the surface of CNF. Thereby, it enhanced the visible-light harvesting. The prepared Fe@V-CNF had remarkable light absorption in the visible region. It demonstrated much higher photocatalytic efficiency of photodegradation of organic dyes compared with the pure CNF and vanadium oxide embedded CNF (V-CNF). Notably, Fe@V-CNF achieved 99.9% dye degradation within 15-20 min. And, it could be conveniently recycled due to its one-dimensional nanostructural property. PMID:24407677

  4. One-dimensional porous nanofibers of Co3O4 on the carbon matrix from human hair with superior lithium ion storage performance

    PubMed Central

    Tan, Yanli; Gao, Qiuming; Yang, Chunxiao; Yang, Kai; Tian, Weiqian; Zhu, Lihua

    2015-01-01

    One-dimensional (1D) hierarchical porous nanofibers of Co3O4 possessing of (220) facets on the carbon matrix from human hair (H2@Co3O4) with 20–30 nm in width and 3–5 μm in length are prepared by a facile solvothermal and calcination approach. The well crystallized small Co3O4 particles with the diameter of about 8–12 nm were closely aggregated together in the nanofibers. Electrochemical analyses show that the first discharge capacity of H2@Co3O4 electrode is 1368 mAh g−1 at the current density of 0.1 A g−1 based on the total mass of composite. A high reversible capacity of 916 mAh g −1 was obtained over 100 cycles at 0.1 A g−1, presenting a good cycling stability. When cycled at a high current density of 1 and 2 A g−1, the specific capacity of 659 and 573 mAh g−1 could be still achieved, respectively, indicating a superior power capability. PMID:26201874

  5. One-dimensional porous nanofibers of Co3O4 on the carbon matrix from human hair with superior lithium ion storage performance

    NASA Astrophysics Data System (ADS)

    Tan, Yanli; Gao, Qiuming; Yang, Chunxiao; Yang, Kai; Tian, Weiqian; Zhu, Lihua

    2015-07-01

    One-dimensional (1D) hierarchical porous nanofibers of Co3O4 possessing of (220) facets on the carbon matrix from human hair (H2@Co3O4) with 20-30 nm in width and 3-5 μm in length are prepared by a facile solvothermal and calcination approach. The well crystallized small Co3O4 particles with the diameter of about 8-12 nm were closely aggregated together in the nanofibers. Electrochemical analyses show that the first discharge capacity of H2@Co3O4 electrode is 1368 mAh g-1 at the current density of 0.1 A g-1 based on the total mass of composite. A high reversible capacity of 916 mAh g -1 was obtained over 100 cycles at 0.1 A g-1, presenting a good cycling stability. When cycled at a high current density of 1 and 2 A g-1, the specific capacity of 659 and 573 mAh g-1 could be still achieved, respectively, indicating a superior power capability.

  6. One-dimensional porous nanofibers of Co3O4 on the carbon matrix from human hair with superior lithium ion storage performance.

    PubMed

    Tan, Yanli; Gao, Qiuming; Yang, Chunxiao; Yang, Kai; Tian, Weiqian; Zhu, Lihua

    2015-01-01

    One-dimensional (1D) hierarchical porous nanofibers of Co3O4 possessing of (220) facets on the carbon matrix from human hair (H2@Co3O4) with 20-30 nm in width and 3-5 μm in length are prepared by a facile solvothermal and calcination approach. The well crystallized small Co3O4 particles with the diameter of about 8-12 nm were closely aggregated together in the nanofibers. Electrochemical analyses show that the first discharge capacity of H2@Co3O4 electrode is 1368 mAh g(-1) at the current density of 0.1 A g(-1) based on the total mass of composite. A high reversible capacity of 916 mAh g (-1) was obtained over 100 cycles at 0.1 A g(-1), presenting a good cycling stability. When cycled at a high current density of 1 and 2 A g(-1), the specific capacity of 659 and 573 mAh g(-1) could be still achieved, respectively, indicating a superior power capability. PMID:26201874

  7. Electrospinning Directly Synthesized Porous TiO2 Nanofibers Modified by Graphitic Carbon Nitride Sheets for Enhanced Photocatalytic Degradation Activity under Solar Light Irradiation.

    PubMed

    Adhikari, Surya Prasad; Awasthi, Ganesh Prasad; Kim, Han Joo; Park, Chan Hee; Kim, Cheol Sang

    2016-06-21

    We report a direct approach to the fabrication of a composite made of porous TiO2 nanofibers (NFs) and graphitic carbon nitride (g-C3N4) sheets, by means of an angled two-nozzle electrospinning combined with calcination process. Different wt % amounts of g-C3N4 particles in a polymer solution from one nozzle and TiO2 precursors containing the same polymer solution from another nozzle were electrospun and deposited on the collector. Structural characterizations confirm a well-defined morphology of the TiO2/g-C3N4 composite in which the TiO2 NFs are uniformly attached on the g-C3N4 sheet. This proper attachment of TiO2 NFs on the g-C3N4 sheets occurred during calcination. The prepared composites showed the enhanced photocatalytic activity over the photodegradation of rhodamine B and reactive black 5 under natural sunlight. Here, the synergistic effect between the g-C3N4 sheets and the TiO2 NFs having anisotropic properties enhanced the photogenerated electron-hole pair separation and migration, which was confirmed by the measurement of photoluminescence spectra, cyclic voltammograms, and electrochemical impedance spectra. The direct synthesis approach that is established here for such kinds of sheetlike structure and porous NFs composites could provide new insights for the design of high-performance energy conversion catalysts. PMID:27254544

  8. Silicon Whisker and Carbon Nanofiber Composite Anode

    NASA Technical Reports Server (NTRS)

    Ma, Junqing (Inventor); Newman, Aron (Inventor); Lennhoff, John (Inventor)

    2015-01-01

    A carbon nanofiber can have a surface and include at least one crystalline whisker extending from the surface of the carbon nanofiber. A battery anode composition can be formed from a plurality of carbon nanofibers each including a plurality of crystalline whiskers.

  9. A rapid and sensitive method for hydroxyl radical detection on a microfluidic chip using an N-doped porous carbon nanofiber modified pencil graphite electrode.

    PubMed

    Ouyang, Jun; Li, Zhong-Qiu; Zhang, Jing; Wang, Chen; Wang, Jiong; Xia, Xing-Hua; Zhou, Guo-Jun

    2014-07-01

    Hydroxyl radicals (˙OH) play an important role in human diseases. Traditional detection methods are time consuming and require expensive instruments. Here, we present a simple and sensitive method for the detection of hydroxyl radicals on a microfluidic chip using an electrochemical technique. Aniline monomer is electrochemically polymerized on the surface of a pencil graphite electrode and carbonized at 800 °C. The resulting N-doped porous carbon nanofiber-modified pencil graphite electrode is embedded into a microfluidic chip directly as a working electrode. 4-Hydroxybenzoic acid (4-HBA) is selected as the trapping agent owing to its unique 3,4-DHBA product and high trapping efficiency. A low detection limit of 1.0 × 10(-6) M is achieved on the microfluidic chip. As a demonstration, the microfluidic chip is successfully utilized for the detection of ˙OH in cigarette smoke. The strong π-π stacking and hydrophobic interactions between the nitrogen-doped carbon materials and the pencil graphite make the modified electrode well-suited for the microfluidic chip. PMID:24834984

  10. Foamed mesoporous carbon/silicon composite nanofiber anode for lithium ion batteries

    NASA Astrophysics Data System (ADS)

    Wang, Yuxin; Wen, Xiufang; Chen, Juan; Wang, Shengnian

    2015-05-01

    A new porous composite nanofiber manufacturing route, combining electrospinning and foaming processes, was developed. In this process, aluminum acetylacetonate (AACA) was introduced as the foaming agent in nanofibers made of polyacrylonitrile (PAN)/silicon (Si) nanoparticles. PAN/Si composite nanofibers were first produced through an electrospinning process and mesopores were then generated by foaming nanofibers via AACA sublimation. After further carbonization, the obtained mesoporous carbon/silicon composite nanofiber mats were tested as the anode material for lithium ion batteries. Within this composite anode, mesopores provide needed buffering space to accommodate the large volume expansion and consequent stress induced inside silicon during lithiation. This effectively mitigates silicon pulverization issue and helps achieve higher reversible capacity and better capacity retention in later battery tests when compared with anodes made of nonporous composites nanofibers and carbon nanofibers alone.

  11. WAXS investigations on Polyethylene -- Carbon Nanofibers Composites

    NASA Astrophysics Data System (ADS)

    Jones, Brian; Li, Jianhua; Benitez, Rogelio; Lozano, Karen; Chipara, Mircea; Cristian Chipara, Alin; Dorina Chipara, Magdalena; Sellmyer, David J.

    2008-03-01

    Nanocomposites have been obtained by high-shear mixing of isotactic polyethylene with various amounts of purified nanofiller (vapor grown carbon nanofibers type PR-24AG from Pyrograf Products, Inc) by utilizing a HAAKE Rheomix at 65 rpm and 180 ^oC for 9 min followed by an additional mixing at 90 rpm for 5 min. Composites loaded with various amounts of vapor grown carbon nanofibers have been prepared. Various spectroscopic techniques have been used to assess the interactions between the polymeric matrix and carbon nanofibers. Wide angle X - Ray scattering investigations focused on the effect of carbon nanofibers on the crystalline phases of polypropylene and on the overall crystallinity degree of the polymeric matrix. This research aims at a better understanding of the nature and structure of the polymer -- carbon nanofibers interface.

  12. Occupational Exposure to Carbon Nanotubes and Nanofibers

    MedlinePlus

    ... Current Intelligence Bulletin 65: Occupational Exposure to Carbon Nanotubes and Nanofibers Recommend on Facebook Tweet Share Compartir ... composed of engineered nanoparticles, such as metal oxides, nanotubes, nanowires, quantum dots, and carbon fullerenes (buckyballs), among ...

  13. Spectroscopic Investigations on Polypropylene -- Carbon Nanofibers Composites

    NASA Astrophysics Data System (ADS)

    Chipara, Mircea; Brian, Jones; Lozano, Karen; Villareal, John R.; Cristian Chipara, Alin; Hernandez, Anna; Dorina Chipara, Magdalena; Sellmyer, David J.

    2008-03-01

    Nanocomposites were obtained by high-shear mixing of isotactic polypropylene (Marlex HLN-120-01; Philips Sumika Polypropylene Company) with various amounts of vapor grown carbon nanofibers (PR-24AG; Pyrograf Products, Inc) by utilizing a HAAKE Rheomix at 65 rpm and 180 ^oC for 9 min followed by an additional mixing at 90 rpm for 5 min. Composites loaded with various amounts of vapor grown carbon nanofibers have been prepared. Wide angle X-Ray scattering investigations focus on the effect of carbon nanofibers on the crystalline phases of polypropylene and on the overall crystallinity degree of the polymeric matrix. Raman spectroscopy analysis concentrates on D and G bands. X-band electron spin resonance investigations aim at a better understanding of the purity of carbon nanofibers and of the ratio between conducting and paramagnetic.

  14. Metal filled porous carbon

    DOEpatents

    Gross, Adam F.; Vajo, John J.; Cumberland, Robert W.; Liu, Ping; Salguero, Tina T.

    2011-03-22

    A porous carbon scaffold with a surface and pores, the porous carbon scaffold containing a primary metal and a secondary metal, where the primary metal is a metal that does not wet the surface of the pores of the carbon scaffold but wets the surface of the secondary metal, and the secondary metal is interspersed between the surface of the pores of the carbon scaffold and the primary metal.

  15. Electrospun Carbon Nanotube-Reinforced Nanofiber.

    PubMed

    Kim, Sung Mm; Hee Kim, Sung; Choi, Myong Soo; Lee, Jun Young

    2016-03-01

    We fabricated multi-walled carbon nanotube (MWNT) reinforced polyurethane (PU) nanofiber (MWNT-PU) web via electrospinning. In order to optimize the electrospinning conditions, we investigated the effects of various parameters including kind of solvent, viscosity of the spinning solution, and flow rate on the spinnability and properties of nanofiber. N,N-dimethylformamide (DMF), tetrahydrofuran (THF) and their mixture with various volume ratio were used as the spinning solvent. Morphology of the nanofiber was studied using scanning electron microscope (SEM) and transmission electron microscope (TEM), confirming successful fabrication of MWNT-PU nanofiber web with uniform dispersion of MWNT in longitudinal direction of the fiber. The MWNT-PU nanofiber web exhibited two times higher tensile strength than PU nanofiber web. We also fabricated electrically conducting MWNT-PU nanofiber web by coating poly(3,4-ehtylenedioxythiophene) (PEDOT) on the surface of MWNT-PU nanofiber web for electromagnetic interference (EMI) shielding application. The electromagnetic interference shielding effectiveness (EMI SE) was quite high as 25 dB in the frequency range from 50 MHz to 10 GHz. PMID:27455732

  16. Facile Synthesis of Porous Silicon Nanofibers by Magnesium Reduction for Application in Lithium Ion Batteries.

    PubMed

    Cho, Daehwan; Kim, Moonkyoung; Hwang, Jeonghyun; Park, Jay Hoon; Joo, Yong Lak; Jeong, Youngjin

    2015-12-01

    We report a facile fabrication of porous silicon nanofibers by a simple three-stage procedure. Polymer/silicon precursor composite nanofibers are first fabricated by electrospinning, a water-based spinning dope, which undergoes subsequent heat treatment and then reduction using magnesium to be converted into porous silicon nanofibers. The porous silicon nanofibers are coated with a graphene by using a plasma-enhanced chemical vapor deposition for use as an anode material of lithium ion batteries. The porous silicon nanofibers can be mass-produced by a simple and solvent-free method, which uses an environmental-friendly polymer solution. The graphene-coated silicon nanofibers show an improved cycling performance of a capacity retention than the pure silicon nanofibers due to the suppression of the volume change and the increase of electric conductivity by the graphene. PMID:26510445

  17. Facile Synthesis of Porous Silicon Nanofibers by Magnesium Reduction for Application in Lithium Ion Batteries

    NASA Astrophysics Data System (ADS)

    Cho, Daehwan; Kim, Moonkyoung; Hwang, Jeonghyun; Park, Jay Hoon; Joo, Yong Lak; Jeong, Youngjin

    2015-10-01

    We report a facile fabrication of porous silicon nanofibers by a simple three-stage procedure. Polymer/silicon precursor composite nanofibers are first fabricated by electrospinning, a water-based spinning dope, which undergoes subsequent heat treatment and then reduction using magnesium to be converted into porous silicon nanofibers. The porous silicon nanofibers are coated with a graphene by using a plasma-enhanced chemical vapor deposition for use as an anode material of lithium ion batteries. The porous silicon nanofibers can be mass-produced by a simple and solvent-free method, which uses an environmental-friendly polymer solution. The graphene-coated silicon nanofibers show an improved cycling performance of a capacity retention than the pure silicon nanofibers due to the suppression of the volume change and the increase of electric conductivity by the graphene.

  18. Fractal Analysis of Gas Diffusion in Porous Nanofibers

    NASA Astrophysics Data System (ADS)

    Xiao, Boqi; Fan, Jintu; Wang, Zongchi; Cai, Xin; Zhao, Xige

    2015-02-01

    In this study, with the consideration of pore size distribution and tortuosity of capillaries, the analytical model for gas diffusivity of porous nanofibers is derived based on fractal theory. The proposed fractal model for the normalized gas diffusivity (De/D0) is found to be a function of the porosity, the area fractal dimensions of pore and the fractal dimension of tortuous capillaries. It is found that the normalized gas diffusivity decreases with increasing of the tortuosity fractal dimension. However, the normalized gas diffusivity is positively correlated with the porosity. The prediction of the proposed fractal model for porous nanofibers with porosity less than 0.75 is highly consistent with the experimental and analytical results found in the literature. The model predictions are compared with the previously reported experimental data, and are in good agreement between the model predictions and experimental data is found. The validity of the present model is thus verified. Every parameter of the proposed formula of calculating the normalized gas diffusivity has clear physical meaning. The proposed fractal model can reveal the physical mechanisms of gas diffusion in porous nanofibers.

  19. Surface Characterization and Functionalization of Carbon Nanofibers

    SciTech Connect

    Klein, Kate L; Melechko, Anatoli Vasilievich; McKnight, Timothy E; Retterer, Scott T; Rack, Philip D; Fowlkes, Jason Davidson; Joy, David Charles; Simpson, Michael L

    2008-01-01

    Carbon nanofibers are high-aspect ratio graphitic materials that have been investigated for numerous applications due to their unique physical properties such as high strength, low density, metallic conductivity, tunable morphology, chemical and environmental stability, as well as compatibility with organochemical modification. Surface studies are extremely important for nanomaterials because not only is the surface structurally and chemically quite different from the bulk, but its properties tend to dominate at the nanoscale due to the drastically increased surface-to-volume ratio. This review surveys recent developments in surface analysis techniques used to characterize the surface structure and chemistry of carbon nanofibers and related carbon materials. These techniques include scanning probe microscopy, infrared and electron spectroscopy, electron microscopy, ion spectrometry, temperature programmed desorption and atom probe analysis. In addition, this article evaluates the methods used to modify the surface of carbon nanofibers in order to enhance their functionality to perform across an exceedingly diverse application space.

  20. Large-Scale and Selective Synthesis of Carbon Nanofiber Bundles, Curved Carbon Nanofibers and Helical Carbon Nanofibers.

    PubMed

    Qi, X S; Ding, Q; Zhong, W; Deng, C Y; Du, Y W

    2015-03-01

    Through the pyrolysis of acetylene at 250 °C, large quantities of carbon nanofiber bundles (CNFBs), curved carbon nanofibers (CCNFs) and helical carbon nanofibers (HCNFs) can be synthesized selectively by controlling the Fe:Cu molar ratio of Fe-Cu nanoparticles. In this study, the systematic experimental results indicated that the Cu content in the Fe-Cu nanoparticles and pyrolysis temperature had great impact on the yield and structure of the final samples. Moreover, the transmission electron microscopic observation indicated that the catalyst nanoparticles were enwrapped tightly by graphite layers, and the obtained HCNFs show good magnetic property. Compared to the methods reported in the literature, the approach described herein has the advantages of being simple, low-cost, and environment-friendly. It is suitable for the controllable and mass production of CNFBs, CCNFs and HCNFs. PMID:26413672

  1. Purification process for vertically aligned carbon nanofibers

    NASA Technical Reports Server (NTRS)

    Nguyen, Cattien V.; Delziet, Lance; Matthews, Kristopher; Chen, Bin; Meyyappan, M.

    2003-01-01

    Individual, free-standing, vertically aligned multiwall carbon nanotubes or nanofibers are ideal for sensor and electrode applications. Our plasma-enhanced chemical vapor deposition techniques for producing free-standing and vertically aligned carbon nanofibers use catalyst particles at the tip of the fiber. Here we present a simple purification process for the removal of iron catalyst particles at the tip of vertically aligned carbon nanofibers derived by plasma-enhanced chemical vapor deposition. The first step involves thermal oxidation in air, at temperatures of 200-400 degrees C, resulting in the physical swelling of the iron particles from the formation of iron oxide. Subsequently, the complete removal of the iron oxide particles is achieved with diluted acid (12% HCl). The purification process appears to be very efficient at removing all of the iron catalyst particles. Electron microscopy images and Raman spectroscopy data indicate that the purification process does not damage the graphitic structure of the nanotubes.

  2. Highly porous 3D nanofiber scaffold using an electrospinning technique.

    PubMed

    Kim, Geunhyung; Kim, WanDoo

    2007-04-01

    A successful 3D tissue-engineering scaffold must have a highly porous structure and good mechanical stability. High porosity and optimally designed pore size provide structural space for cell accommodation and migration and enable the exchange of nutrients between the scaffold and environment. Poly(epsilon-carprolactone) fibers were electrospun using an auxiliary electrode and chemical blowing agent (BA), and characterized according to porosity, pore size, and their mechanical properties. We also investigated the effect of the BA on the electrospinning processability. The growth characteristic of human dermal fibroblasts cells cultured in the webs showed the good adhesion with the blown web relative to a normal electrospun mat. The blown nanofiber web had good tensile properties and high porosity compared to a typical electrospun nanofiber scaffold. PMID:16924612

  3. Tunable Graphitic Carbon Nano-Onions Development in Carbon Nanofibers for Multivalent Energy Storage

    SciTech Connect

    Schwarz, Haiqing L.

    2016-01-01

    We developed a novel porous graphitic carbon nanofiber material using a synthesis strategy combining electrospinning and catalytic graphitization. RF hydrogel was used as carbon precursors, transition metal ions were successfully introduced into the carbon matrix by binding to the carboxylate groups of a resorcinol derivative. Transition metal particles were homogeneously distributed throughout the carbon matrix, which are used as in-situ catalysts to produce graphitic fullerene-like nanostructures surrounding the metals. The success design of graphitic carbons with enlarged interlayer spacing will enable the multivalent ion intercalation for the development of multivalent rechargeable batteries.

  4. Carbon nano-chain and carbon nano-fibers based gas diffusion layers for proton exchange membrane fuel cells

    NASA Astrophysics Data System (ADS)

    Kannan, Arunachala M.; Munukutla, Lakshmi

    Gas diffusion layers (GDL) for proton exchange membrane fuel cell have been developed using a partially ordered graphitized nano-carbon chain (Pureblack ® carbon) and carbon nano-fibers. The GDL samples' characteristics such as, surface morphology, surface energy, bubble-point pressure and pore size distribution were characterized using electron microscope, inverse gas chromatograph, gas permeability and mercury porosimetry, respectively. Fuel cell performance of the GDLs was evaluated using single cell with hydrogen/air at ambient pressure, 70 °C and 100% RH. The GDLs with combination of vapor grown carbon nano-fibers with Pureblack carbon showed significant improvement in mechanical robustness as well as fuel cell performance. The micro-porous layer of the GDLs as seen under scanning electron microscope showed excellent surface morphology showing the reinforcement with nano-fibers and the surface homogeneity without any cracks.

  5. Preparation and characterization of silica nanoparticulate polyacrylonitrile composite and porous nanofibers

    NASA Astrophysics Data System (ADS)

    Ji, Liwen; Saquing, Carl; Khan, Saad A.; Zhang, Xiangwu

    2008-02-01

    In this study, polyacrylonitrile (PAN) composite nanofibers containing different amounts of silica nanoparticulates have been obtained via electrospinning. The surface morphology, thermal properties and crystal structure of PAN/silica nanofibers are characterized using attenuated total reflection Fourier transform infrared (ATR-FTIR) spectroscopy, wide-angle x-ray diffraction (WAXD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and differential scanning calorimetry (DSC). The results indicate that the addition of silica nanoparticulates affects the structure and properties of the nanofibers. In addition to PAN/silica composite nanofibers, porous PAN nanofibers have been prepared by selective removal of the silica component from PAN/silica composite nanofibers using hydrofluoric (HF) acid. ATR-FTIR and thermal gravimetric analysis (TGA) experiments validate the removal of silica nanoparticulates by HF acid, whereas SEM and TEM results reveal that the porous nanofibers obtained from composite fibers with higher silica contents exhibited more nonuniform surface morphology. The Brunauer-Emmett-Teller (BET) surface area of porous PAN nanofibers made from PAN/silica (5 wt%) composite precursors is higher than that of pure nonporous PAN nanofibers.

  6. A synergetic description of the carbon nanofiber growth.

    SciTech Connect

    Merkulov, Igor A; Simpson, Michael L; Klein, Kate L

    2009-01-01

    The self-consistent mathematical model has been developed for the catalytic chemical vapor deposition carbon nanofiber growth. This model includes the balance equation for the carbon transport through the catalyst and the equation for mechanical and chemical balance in the catalyst nanofiber system. It is demonstrated that the most important parameter that governs the catalyst-nanofiber growth system behavior is the difference of the carbon chemical potentials in catalyst and nanofiber. This parameter determines the carbon transport to the nanofiber. It is also responsible for the catalyst shape and topology of the interface between catalyst and nanofiber. Model solutions are in agreement with numerous experimental results. The model can be used for planning new experiments and explaining existing results. It leaves the opportunity for more precise and complicated mathematical calculations of different parts of the growth process.

  7. The synthesis of titanium carbide-reinforced carbon nanofibers

    NASA Astrophysics Data System (ADS)

    Zhu, Pinwen; Hong, Youliang; Liu, Bingbing; Zou, Guangtian

    2009-06-01

    Tailoring hard materials into nanoscale building blocks can greatly extend the applications of hard materials and, at the same time, also represents a significant challenge in the field of nanoscale science. This work reports a novel process for the preparation of carbon-based one-dimensional hard nanomaterials. The titanium carbide-carbon composite nanofibers with an average diameter of 90 nm are prepared by an electrospinning technique and a high temperature pyrolysis process. A composite solution containing polyacrylonitrile and titanium sources is first electrospun into the composite nanofibers, which are subsequently pyrolyzed to produce the desired products. The x-ray diffraction pattern and transmission electron microscopy results show that the main phase of the as-synthesized nanofibers is titanium carbide. The Raman analyses show that the composite nanofibers have low graphite clusters in comparison with the pure carbon nanofibers originating from the electrospun polyacrylonitrile nanofibers. The mechanical property tests demonstrate that the titanium carbide-carbon nanofiber membranes have four times higher tensile strength than the carbon nanofiber membranes, and the Young's modulus of the titanium carbide-carbon nanofiber membranes increases in direct proportion to the titanium quantity.

  8. Synthesis of carbon nanofibers on copper particles

    NASA Astrophysics Data System (ADS)

    Kol'tsova, T. S.; Larionova, T. V.; Shusharina, N. N.; Tolochko, O. V.

    2015-08-01

    We analyze the synthesis of carbon nanostructures from the gas phase (mixture of acetylene or ethylene with hydrogen) on the surface of copper particles without using other catalysts. The synthesized structures (multilayer graphene and carbon nanofibers) are analyzed by transmission electron microscopy and Raman scattering. It is shown that the fiber structure is determined by the C: H ratio in the gas phase. The kinetics of synthesis is analyzed in terms of the formal kinetics of conversion in accordance with the Johnson—Mehl—Avrami equation.

  9. Electrospun La0.8Sr0.2MnO3 nanofibers for a high-temperature electrochemical carbon monoxide sensor

    NASA Astrophysics Data System (ADS)

    Zhi, Mingjia; Koneru, Anveeksh; Yang, Feng; Manivannan, Ayyakkannu; Li, Jing; Wu, Nianqiang

    2012-08-01

    Lanthanum strontium manganite (La0.8Sr0.2MnO3, LSM) nanofibers have been synthesized by the electrospinning method. The electrospun nanofibers are intact without morphological and structural changes after annealing at 1050 °C. The LSM nanofibers are employed as the sensing electrode of an electrochemical sensor with yttria-stabilized zirconia (YSZ) electrolyte for carbon monoxide detection at high temperatures over 500 °C. The electrospun nanofibers form a porous network electrode, which provides a continuous pathway for charge transport. In addition, the nanofibers possess a higher specific surface area than conventional micron-sized powders. As a result, the nanofiber electrode exhibits a higher electromotive force and better electro-catalytic activity toward CO oxidation. Therefore, the sensor with the nanofiber electrode shows a higher sensitivity, lower limit of detection and faster response to CO than a sensor with a powder electrode.

  10. Synthesis of aluminum oxy-hydroxide nanofibers from porous anodic alumina.

    PubMed

    Jha, Himendra; Kikuchi, Tatsuya; Sakairi, Masatoshi; Takahashi, Hideaki

    2008-10-01

    A novel method for the synthesis of aluminum oxy-hydroxide nanofibers from a porous anodic oxide film of aluminum is demonstrated. In the present method, the porous anodic alumina not only acts as a template, but also serves as the starting material for the synthesis. The porous anodic alumina film is hydrothermally treated for pore-sealing, which forms aluminum oxy-hydroxide inside the pores of the oxide film as well as on the surface of the film. The hydrothermally sealed porous oxide film is immersed in the sodium citrate solution, which selectively etches the porous aluminum oxide from the film, leaving the oxy-hydroxide intact. The method is simple and gives highly uniform aluminum oxy-hydroxide nanofibers. Moreover, the diameter of the nanofibers can be controlled by controlling the pore size of the porous anodic alumina film, which depends on the anodizing conditions. Nanofibers with diameters of about 38-85 nm, having uniform shape and size, were successfully synthesized using the present method. PMID:21832599

  11. Enhancement of conductivity by diameter control of polyimide-based electrospun carbon nanofibers.

    PubMed

    Xuyen, Nguyen Thi; Ra, Eun Ju; Geng, Hong-Zhang; Kim, Ki Kang; An, Kay Hyeok; Lee, Young Hee

    2007-10-01

    Oxydianiline-pyromellitic dianhydride poly(amic acid) (ODA-PMDA PAA) was polymerized with a catalyst support of triethyl amine for controlling molecular weight. This polymer was used for electrospinning in the preparation of PAA nanofibers, a precursor of carbon nanofibers. Here the amount of catalyst and concentration of PAA solution were optimized to produce polyimide-based carbon nanofibers approximately 80 nm in diameter. The effects of molecular weight of PAA, bias voltage, and spinning rate on the morphology of electrospun PAA and polyimide nanofibers have been evaluated. We showed that the conductivity of the carbon nanofiber mat decreased with increasing nanofiber diameter, where the conductivity of polyimide-based carbon nanofiber mat was much higher than those of other types of carbon nanofiber mat. The key ingredient to increase conductivity in a carbon nanofiber mat was found to be the number of cross junctions between nanofibers. PMID:17850139

  12. Interfacial engineering of carbon nanofiber-graphene-carbon nanofiber heterojunctions in flexible lightweight electromagnetic shielding networks.

    PubMed

    Song, Wei-Li; Wang, Jia; Fan, Li-Zhen; Li, Yong; Wang, Chan-Yuan; Cao, Mao-Sheng

    2014-07-01

    Lightweight carbon materials of effective electromagnetic interference (EMI) shielding have attracted increasing interest because of rapid development of smart communication devices. To meet the requirement in portable electronic devices, flexible shielding materials with ultrathin characteristic have been pursued for this purpose. In this work, we demonstrated a facile strategy for scalable fabrication of flexible all-carbon networks, where the insulting polymeric frames and interfaces have been well eliminated. Microscopically, a novel carbon nanofiber-graphene nanosheet-carbon nanofiber (CNF-GN-CNF) heterojunction, which plays the dominant role as the interfacial modifier, has been observed in the as-fabricated networks. With the presence of CNF-GN-CNF heterojunctions, the all-carbon networks exhibit much increased electrical properties, resulting in the great enhancement of EMI shielding performance. The related mechanism for engineering the CNF interfaces based on the CNF-GN-CNF heterojunctions has been discussed. Implication of the results suggests that the lightweight all-carbon networks, whose thickness and density are much smaller than other graphene/polymer composites, present more promising potential as thin shielding materials in flexible portable electronics. PMID:24914611

  13. Catalytic Growth of Macroscopic Carbon Nanofibers Bodies with Activated Carbon

    SciTech Connect

    Abdullah, N.; Muhammad, I. S.; Hamid, S. B. Abd.; Rinaldi, A.; Su, D. S.; Schlogl, R.

    2009-06-01

    Carbon-carbon composite of activated carbon and carbon nanofibers have been synthesized by growing Carbon nanofiber (CNF) on Palm shell-based Activated carbon (AC) with Ni catalyst. The composites are in an agglomerated shape due to the entanglement of the defective CNF between the AC particles forming a macroscopic body. The macroscopic size will allow the composite to be used as a stabile catalyst support and liquid adsorbent. The preparation of CNT/AC nanocarbon was initiated by pre-treating the activated carbon with nitric acid, followed by impregnation of 1 wt% loading of nickel (II) nitrate solutions in acetone. The catalyst precursor was calcined and reduced at 300 deg. C for an hour in each step. The catalytic growth of nanocarbon in C{sub 2}H{sub 4}/H{sub 2} was carried out at temperature of 550 deg. C for 2 hrs with different rotating angle in the fluidization system. SEM and N{sub 2} isotherms show the level of agglomeration which is a function of growth density and fluidization of the system. The effect of fluidization by rotating the reactor during growth with different speed give a significant impact on the agglomeration of the final CNF/AC composite and thus the amount of CNFs produced. The macrostructure body produced in this work of CNF/AC composite will have advantages in the adsorbent and catalyst support application, due to the mechanical and chemical properties of the material.

  14. Improved fire retardancy of thermoset composites modified with carbon nanofibers

    NASA Astrophysics Data System (ADS)

    Zhao, Zhongfu; Gou, Jan

    2009-01-01

    Multifunctional thermoset composites were made from polyester resin, glass fiber mats and carbon nanofiber sheets (CNS). Their flaming behavior was investigated with cone calorimeter under well-controlled combustion conditions. The heat release rate was lowered by pre-planting carbon nanofiber sheets on the sample surface with the total fiber content of only 0.38 wt.%. Electron microscopy showed that carbon nanofiber sheet was partly burned and charred materials were formed on the combusting surface. Both the nanofibers and charred materials acted as an excellent insulator and/or mass transport barrier, improving the fire retardancy of the composite. This behavior agrees well with the general mechanism of fire retardancy in various nanoparticle-thermoplastic composites.

  15. A miniature microbial fuel cell with conducting nanofibers-based 3D porous biofilm

    NASA Astrophysics Data System (ADS)

    Jiang, Huawei; Halverson, Larry J.; Dong, Liang

    2015-12-01

    Miniature microbial fuel cell (MFC) technology has received growing interest due to its potential applications in high-throughput screening of bacteria and mutants to elucidate mechanisms of electricity generation. This paper reports a novel miniature MFC with an improved output power density and short startup time, utilizing electrospun conducting poly(3,4-ethylenedioxythiophene) (PEDOT) nanofibers as a 3D porous anode within a 12 μl anolyte chamber. This device results in 423 μW cm-3 power density based on the volume of the anolyte chamber, using Shewanella oneidensis MR-1 as a model biocatalyst without any optimization of bacterial culture. The device also excels in a startup time of only 1hr. The high conductivity of the electrospun nanofibers makes them suitable for efficient electron transfer. The mean pore size of the conducting nanofibers is several micrometers, which is favorable for bacterial penetration and colonization of surfaces of the nanofibers. We demonstrate that S. oneidensis can fully colonize the interior region of this nanofibers-based porous anode. This work represents a new attempt to explore the use of electrospun PEDOT nanofibers as a 3D anode material for MFCs. The presented miniature MFC potentially will provide a high-sensitivity, high-throughput tool to screen suitable bacterial species and mutant strains for use in large-size MFCs.

  16. Supercapacitor Electrodes Based on High-Purity Electrospun Polyaniline and Polyaniline-Carbon Nanotube Nanofibers.

    PubMed

    Simotwo, Silas K; DelRe, Christopher; Kalra, Vibha

    2016-08-24

    Freestanding, binder-free supercapacitor electrodes based on high-purity polyaniline (PANI) nanofibers were fabricated via a single step electrospinning process. The successful electrospinning of nanofibers with an unprecedentedly high composition of PANI (93 wt %) was made possible due to blending ultrahigh molecular weight poly(ethylene oxide) (PEO) with PANI in solution to impart adequate chain entanglements, a critical requirement for electrospinning. To further enhance the conductivity and stability of the electrodes, a small concentration of carbon nanotubes (CNTs) was added to the PANI/PEO solution prior to electrospinning to generate PANI/CNT/PEO nanofibers (12 wt % CNTs). Scanning electron microscopy (SEM) and Brunauer-Emmett-Teller (BET) porosimetry were conducted to characterize the external morphology of the nanofibers. The electrospun nanofibers were further probed by transmission electron microscopy (TEM), X-ray diffraction (XRD), and Fourier transform infrared spectroscopy (FT-IR). The electroactivity of the freestanding PANI and PANI/CNT nanofiber electrodes was examined using cyclic voltammetry, galvanostatic charge-discharge, and electrochemical impedance spectroscopy. Competitive specific capacitances of 308 and 385 F g(-1) were achieved for PANI and PANI-CNT based electrodes, respectively, at a current density of 0.5 A g(-1). Moreover, specific capacitance retentions of 70 and 81.4% were observed for PANI and PANI-CNT based electrodes, respectively, after 1000 cycles. The promising electrochemical performance of the fabricated electrodes, we believe, stems from the porous 3-D electrode structure characteristic of the nonwoven interconnected nanostructures. The interconnected nanofiber network facilitates efficient electron conduction while the inter- and intrafiber porosity enable excellent electrolyte penetration within the polymer matrix, allowing fast ion transport to the active sites. PMID:27467445

  17. Improvement of thermal contact resistance by carbon nanotubes and nanofibers

    NASA Technical Reports Server (NTRS)

    Chuang, Helen F.; Cooper, Sarah M.; Meyyappan, M.; Cruden, Brett A.

    2004-01-01

    Interfacial thermal resistance results of various nanotube and nanofiber coatings, prepared by chemical vapor deposition (CVD) methods, are reported at relatively low clamping pressures. The five types of samples examined include multi-walled and single-walled nanotubes growth by CVD, multi-walled nanotubes grown by plasma enhanced CVD (PECVD) and carbon nanofibers of differing aspect ratio grown by PECVD. Of the samples examined, only high aspect ratio nanofibers and thermally grown multi-walled nanotubes show an improvement in thermal contact resistance. The improvement is approximately a 60% lower thermal resistance than a bare Si-Cu interface and is comparable to that attained by commercially available thermal interface materials.

  18. Patterned Growth of Carbon Nanotubes or Nanofibers

    NASA Technical Reports Server (NTRS)

    Delzeit, Lance D.

    2004-01-01

    A method and apparatus for the growth of carbon nanotubes or nanofibers in a desired pattern has been invented. The essence of the method is to grow the nanotubes or nanofibers by chemical vapor deposition (CVD) onto a patterned catalyst supported by a substrate. The figure schematically depicts salient aspects of the method and apparatus in a typical application. A substrate is placed in a chamber that contains both ion-beam sputtering and CVD equipment. The substrate can be made of any of a variety of materials that include several forms of silicon or carbon, and selected polymers, metals, ceramics, and even some natural minerals and similar materials. Optionally, the substrate is first coated with a noncatalytic metal layer (which could be a single layer or could comprise multiple different sublayers) by ion-beam sputtering. The choice of metal(s) and thickness(es) of the first layer (if any) and its sublayers (if any) depends on the chemical and electrical properties required for subsequent deposition of the catalyst and the subsequent CVD of the carbon nanotubes. A typical first-sublayer metal is Pt, Pd, Cr, Mo, Ti, W, or an alloy of two or more of these elements. A typical metal for the second sublayer or for an undivided first layer is Al at a thickness .1 nm or Ir at a thickness .5 nm. Proper choice of the metal for a second sublayer of a first layer makes it possible to use a catalyst that is chemically incompatible with the substrate. In the next step, a mask having holes in the desired pattern is placed over the coated substrate. The catalyst is then deposited on the coated substrate by ion-beam sputtering through the mask. Optionally, the catalyst could be deposited by a technique other than sputtering and/or patterned by use of photolithography, electron- beam lithography, or another suitable technique. The catalytic metal can be Fe, Co, Ni, or an alloy of two or more of these elements, deposited to a typical thickness in the range from 0.1 to 20 nm.

  19. Functionalized carbon nanotubes and nanofibers for biosensing applications

    SciTech Connect

    Wang, Jun; Lin, Yuehe

    2008-07-30

    This review summarizes the recent advances of carbon nanotube (CNT) and carbon nanofiber (CNF)-based electrochemical biosensors with an emphasis on the applications of CNTs. Carbon nanotubes and carbon nanofibers have unique electric, electrocatalytic, and mechanical properties which make them efficient materials for the use in electrochemical biosensor development. In this article, the functionalization of CNTs for biosensors is simply discussed. The electrochemical biosensors based on CNT and their various applications, e.g., measurement of small biological molecules and environmental pollutants, detection of DNA, and immunosensing of disease biomarkers, are reviewed. Moreover, the development of carbon nanofiber-based electrochemical biosensors and their applications are outlined. Finally, some challenges are discussed in the conclusion.

  20. Carbon Nanofiber Nanoelectrodes for Biosensing Applications

    NASA Technical Reports Server (NTRS)

    Koehne, Jessica Erin

    2014-01-01

    A sensor platform based on vertically aligned carbon nanofibers (CNFs) has been developed. Their inherent nanometer scale, high conductivity, wide potential window, good biocompatibility and well-defined surface chemistry make them ideal candidates as biosensor electrodes. Here, we report two studies using vertically aligned CNF nanoelectrodes for biomedical applications. CNF arrays are investigated as neural stimulation and neurotransmitter recording electrodes for application in deep brain stimulation (DBS). Polypyrrole coated CNF nanoelectrodes have shown great promise as stimulating electrodes due to their large surface area, low impedance, biocompatibility and capacity for highly localized stimulation. CNFs embedded in SiO2 have been used as sensing electrodes for neurotransmitter detection. Our approach combines a multiplexed CNF electrode chip, developed at NASA Ames Research Center, with the Wireless Instantaneous Neurotransmitter Concentration Sensor (WINCS) system, developed at the Mayo Clinic. Preliminary results indicate that the CNF nanoelectrode arrays are easily integrated with WINCS for neurotransmitter detection in a multiplexed array format. In the future, combining CNF based stimulating and recording electrodes with WINCS may lay the foundation for an implantable smart therapeutic system that utilizes neurochemical feedback control while likely resulting in increased DBS application in various neuropsychiatric disorders. In total, our goal is to take advantage of the nanostructure of CNF arrays for biosensing studies requiring ultrahigh sensitivity, high-degree of miniaturization, and selective biofunctionalization.

  1. Silane coupling agent structures on carbon nanofibers.

    PubMed

    Palencia, Cristina; Rubio, Juan; Rubio, Fausto; Fierro, José Luis G; Oteo, José Luis

    2011-05-01

    Carbon nanofibers (CNFs) are considered ideal materials for reinforcing polymers due to their excellent mechanical properties, among others. In order to obtain composites of optimal properties the clue is to enhance the interaction between reinforcement (CNFs) and polymer matrix. Surface modification of CNFs with silane coupling agents (SCAs) has revealed as one of the most interesting methods. The silanization process has been carried out mixing at room temperature and for one minute the hydrolysed silane with CNFs. We have use four different SCAs: 3-aminopropyltriethoxyxilane (APS), 3-aminopropyltrimethoxysilane (AMMO), N-(2-aminoethyl)-3-(aminopropyltrimethoxysilane) (DAMO), and 3-glycidoxypropyltrimethoxysilane (GLYMO), in order to elucidate the SCA-CNFs interaction and the silane structures formed on CNFs surface. XPS and FTIR-ATR techniques have pointed out that each silane adsorbs on CNFs surface through chemical bonding, forming multilayers. Silane nature determines the structure taken on CNFs surface. APS and AMO silanes adsorb taking vertical structures on CNFs surface, while DMO and GMO adsorb on CNFs taking horizontal structures, stabilized by zwitterions formed through H-bonds with hydroxyl groups from CNFs surface. PMID:21780418

  2. Treated Carbon Nanofibers for Storing Energy in Aqueous KOH

    NASA Technical Reports Server (NTRS)

    Firsich, David W.

    2004-01-01

    A surface treatment has been found to enhance the performances of carbon nanofibers as electrode materials for electrochemical capacitors in which aqueous solutions of potassium hydroxide are used as the electrolytes. In the treatment, sulfonic acid groups are attached to edge plane sites on carbon atoms. The treatment is applicable to a variety of carbon nanofibers, including fibrils and both single- and multiple-wall nanotubes. The reason for choosing nanofibers over powders and other forms of carbon is that nanofibers offer greater power features. In previous research, it was found that the surface treatment of carbon nanofibers increased energy-storage densities in the presence of acid electrolytes. Now, it has been found that the same treatment increases energy-storage densities of carbon nanofibers in the presence of alkaline electrolytes when the carbon is paired with a NiOOH electrode. This beneficial effect varies depending on the variety of carbon substrate to which it is applied. It has been conjectured that the sulfonic acid groups, which exist in a deprotonated state in aqueous KOH solutions, undergo reversible electro-chemical reactions that are responsible for the observed increases in energystorage capacities. The increases can be considerable: For example, in one case, nanofibers exhibited a specific capacitance of 34 Farads per gram before treatment and 172 Farads per gram (an increase of about 400 percent) after treatment. The most promising application of this development appears to lie in hybrid capacitors, which are devices designed primarily for storing energy. These devices are designed to be capable of (1) discharge at rates greater than those of batteries and (2) storing energy at densities approaching those of batteries. A hybrid capacitor includes one electrode like that of a battery and one electrode like that of an electrochemical capacitor. For example, a hybrid capacitor could contain a potassium hydroxide solution as the electrolyte

  3. Preparation of Electrically Conductive Polystyrene/Carbon Nanofiber Nanocomposite Films

    ERIC Educational Resources Information Center

    Sun, Luyi; O'Reilly, Jonathan Y.; Tien, Chi-Wei; Sue, Hung-Jue

    2008-01-01

    A simple and effective approach to prepare conductive polystyrene/carbon nanofiber (PS/CNF) nanocomposite films via a solution dispersion method is presented. Inexpensive CNF, which has a structure similar to multi-walled carbon nanotubes, is chosen as a nanofiller in this experiment to achieve conductivity in PS films. A good dispersion is…

  4. Electromagnetic interference shielding characteristics of carbon nanofiber-polymer composites.

    PubMed

    Yang, Yonglai; Guptal, Mool C; Dudley, Kenneth L; Lawrence, Roland W

    2007-02-01

    Electromagnetic interference (EMI) shielding characteristics of carbon nanofiber-polystyrene composites were investigated in the frequency range of 12.4-18 GHz (Ku-band). It was observed that the shielding effectiveness of such composites was frequency independent, and increased with increasing carbon nanofiber loading within Ku-band. The experimental data exhibited that the shielding effectiveness of the polymer composite containing 20 wt% carbon nanofibers could reach more than 36 dB in the measured frequency region, indicating such composites can be applied to the potential EMI shielding materials. In addition, the results showed that the contribution of reflection to the EMI shielding effectiveness was much larger than that of absorption, implying the primary EMI shielding mechanism of such composites was reflection of electromagnetic radiation within Ku-band. PMID:17450793

  5. Morphology of PEG-Stabilized Carbon Nanofibers in Water

    SciTech Connect

    Zhao, Jian; Schaefer, Dale W.

    2009-09-02

    Small-angle light scattering is used to assess the dispersion of poly(ethylene glycol) (PEG)-functionalized carbon nanofibers suspended in water. Analysis of these data elucidates the mechanism by which the functionalized nanofibers are solubilized in water. Linear, tube-like morphology is observed for the PEG-functionalized nanofibers dispersed in water. However, dispersion is not down to the individual tube level as determined by analysis of the light scattering data in conjunction with transmission electron micrographs. Rather, scattering entities are polydisperse side-by-side fiber aggregates (bundles). Because of the presence of water-soluble PEG oligomers on the surfaces of the nanofibers these small-scale aggregates do not agglomerate to form the large-scale clusters that are observed for untreated and acid-treated nanofibers. Acid-treated nanofibers, by contrast, do agglomerate, but in an unusual fashion, showing a 10-h induction period of followed by linear growth of large-scale agglomerates. PEG-functionalization of the acid-treated fibers leads to stabilization by inhibiting formation of the large-scale agglomerates, not by disrupting the side-by-side bundles.

  6. Porous SiO2 nanofiber grafted novel bioactive glass-ceramic coating: A structural scaffold for uniform apatite precipitation and oriented cell proliferation on inert implant.

    PubMed

    Das, Indranee; De, Goutam; Hupa, Leena; Vallittu, Pekka K

    2016-05-01

    A composite bioactive glass-ceramic coating grafted with porous silica nanofibers was fabricated on inert glass to provide a structural scaffold favoring uniform apatite precipitation and oriented cell proliferation. The coating surfaces were investigated thoroughly before and after immersion in simulated body fluid. In addition, the proliferation behavior of fibroblast cells on the surface was observed for several culture times. The nanofibrous exterior of this composite bioactive coating facilitated homogeneous growth of flake-like carbonated hydroxyapatite layer within a short period of immersion. Moreover, the embedded porous silica nanofibers enhanced hydrophilicity which is required for proper cell adhesion on the surface. The cells proliferated well following a particular orientation on the entire coating by the assistance of nanofibrous scaffold-like structural matrix. This newly engineered composite coating was effective in creating a biological structural matrix favorable for homogeneous precipitation of calcium phosphate, and organized cell growth on the inert glass surface. PMID:26952416

  7. Hemocompatible and antibacterial porous membranes with heparinized copper hydroxide nanofibers as separation layer.

    PubMed

    Zhu, Li-Jing; Zhu, Li-Ping; Yi, Zhuan; Jiang, Jin-Hong; Zhu, Bao-Ku; Xu, You-Yi

    2013-10-01

    Here we report the fabrication of a novel heparinized copper hydroxide (Cu(OH)2) nanofiberous membrane with satisfying hemocompatibility and antibacterial properties. The positively charged Cu(OH)2 nanofibers were prepared in a weakly alkaline copper nitrate solution in the presence of 2-aminoethanol. A heparin (Hep) solution was then added dropwise into the solution of nanofibers to immobilize negatively charged heparin onto the Cu(OH)2 nanofibers by electrostatic interaction. A composite Hep@Cu(OH)2 nanofiberous membrane was prepared by filtration and deposition of the heparinized nanofibers onto a polysulfone (PSF) porous membrane. Chemical composition analysis of membrane surface using X-ray photoelectron spectroscopy (XPS) confirmed the successful immobilization of heparin on Cu(OH)2 nanofibers. The amount of immobilized heparin on nanofiberous membrane was determined by a colorimetric assay of toluidine blue dye and the results showed that the amount of immobilized heparin was strongly dependent on the heparin dosage in reaction solution. The results of contact angle measurement indicated that the hydrophilicity of Cu(OH)2 nanofiberous membranes was enhanced by the immobilization of heparin. The adhesion, activation and transmutation of platelets on Hep@Cu(OH)2 membrane were suppressed remarkably due to the introduction of heparin, which suggested that the Hep@Cu(OH)2 membranes had good hemocompatibility. In addition, Cu(OH)2 and Hep@Cu(OH)2 nanofiberous membranes exhibited very good antibacterial activities against Escherichia coli and Staphyloccocus aureus. PMID:23707848

  8. Encapsulation of MnO Nanocrystals in Electrospun Carbon Nanofibers as High-Performance Anode Materials for Lithium-Ion Batteries

    PubMed Central

    Liu, Bin; Hu, Xianluo; Xu, Henghui; Luo, Wei; Sun, Yongming; Huang, Yunhui

    2014-01-01

    A novel and controllable approach is developed for the synthesis of MnO nanocrystals embedded in carbon nanofibers (MnO/CNFs) through an electrospinning process. The as-formed MnO/CNFs have a porous structure with diameters of 100–200 nm and lengths up to several millimeters. When used as an anode material for lithium-ion batteries, the resulting MnO/CNFs exhibit superior electrochemical performances with high specific capacity, good cyclability, and excellent rate capability. The unique porous carbon nanofibers (PCNFs) can not only improve the contact area between the electrode and the electrolyte, but also alleviate the impact of the large volume effect of MnO during the electrochemical cycling. It is expected that the present synthetic strategy can be extended to synthesize other nanostructured oxides encapsulated in carbon nanofibers for extensive energy transfer and storage applications. PMID:24598639

  9. Surface functionalization of carbon nanofibers by sol gel coating of zinc oxide

    NASA Astrophysics Data System (ADS)

    Shao, Dongfeng; Wei, Qufu; Zhang, Liwei; Cai, Yibing; Jiang, Shudong

    2008-08-01

    In this paper the functional carbon nanofibers were prepared by the carbonization of ZnO coated PAN nanofibers to expand the potential applications of carbon nanofibers. Polyacrylonitrile (PAN) nanofibers were obtained by electrospinning. The electrospun PAN nanofibers were then used as substrates for depositing the functional layer of zinc oxide (ZnO) on the PAN nanofiber surfaces by sol-gel technique. The effects of coating, pre-oxidation and carbonization on the surface morphology and structures of the nanofibers were characterized by X-ray diffraction (XRD), Fourier transform infrared (FTIR) and Scanning electron microscopy (SEM), respectively. The results of SEM showed a significant increase of the size of ZnO nanograins on the surface of nanofibers after the treatments of coating, pre-oxidation and carbonization. The observations by SEM also revealed that ZnO nanoclusters were firmly and clearly distributed on the surface of the carbon nanofibers. FTIR examination also confirmed the deposition of ZnO on the surface of carbon nanofibers. The XRD analysis indicated that the crystal structure of ZnO nanograins on the surface of carbon nanofibers.

  10. Plasma-enhanced chemical vapor deposition of multiwalled carbon nanofibers

    NASA Technical Reports Server (NTRS)

    Matthews, Kristopher; Cruden, Brett A.; Chen, Bin; Meyyappan, M.; Delzeit, Lance

    2002-01-01

    Plasma-enhanced chemical vapor deposition is used to grow vertically aligned multiwalled carbon nanofibers (MWNFs). The graphite basal planes in these nanofibers are not parallel as in nanotubes; instead they exhibit a small angle resembling a stacked cone arrangement. A parametric study with varying process parameters such as growth temperature, feedstock composition, and substrate power has been conducted, and these parameters are found to influence the growth rate, diameter, and morphology. The well-aligned MWNFs are suitable for fabricating electrode systems in sensor and device development.

  11. Improvement of thermal contact resistance by carbon nanotubes and nanofibers.

    PubMed

    Chuang, Helen F; Cooper, Sarah M; Meyyappan, M; Cruden, Brett A

    2004-11-01

    Interfacial thermal resistance results of various nanotube and nanofiber coatings, prepared by chemical vapor deposition (CVD) methods, are reported at relatively low clamping pressures. The five types of samples examined include multi-walled and single-walled nanotubes growth by CVD, multi-walled nanotubes grown by plasma enhanced CVD (PECVD) and carbon nanofibers of differing aspect ratio grown by PECVD. Of the samples examined, only high aspect ratio nanofibers and thermally grown multi-walled nanotubes show an improvement in thermal contact resistance. The improvement is approximately a 60% lower thermal resistance than a bare Si-Cu interface and is comparable to that attained by commercially available thermal interface materials. PMID:15656186

  12. Electrochemical Properties of Electrospun Ni Doped Carbon Nanofibers.

    PubMed

    Huang, Yarong; Li, Chunping; Bai, Jie; Huang, Guofang; Sun, Weiyan; Wang, Junzhong

    2016-06-01

    The materials of Ni nanoparticles/carbon nanofibers (Ni NPs/CNFs) and carbon nanofibers (CNFs) were prepared by electrospinning the Ni doped precursor solutions. The Ni doped nanofibers with the diameter of 200-300 nm possess the uniform morphology and smooth surface. These nanofibers were carbonized at 600 degrees C for 2 h. The Ni NPs/CNFs composite was characterized with SEM (scanning electro microscope), XRD (X-ray diffraction) and FT-IR (Infrared spectroscopy). The Ni NPs/CNFs electrode was investigated through the cyclic voltammetry measurement. The average specific capacity was calculated to be 113 F x g(-1) at the scan rate of 2 mV x s(-1). The high specific capacity was larger than the CNFs owing to the Ni NPs. The specific capacity retention also maintains 72% after 5 cycles, suggesting that the electrode possess good reversibility. The Ni NPs/CNFs composite material with excellent electrochemical properties will be a promising material which can be used for energy storage. PMID:27427729

  13. Synthesis and Electrochemical Properties of Carbon Nanofibers and SiO2/Carbon Nanofiber Composite on Ni-Cu/C-Fiber Textiles.

    PubMed

    Nam, Ki-Mok; Park, Heai-Ku; Lee, Chang-Seop

    2015-11-01

    In this study, carbon nanofibers (CNFs) were grown by chemical vapor deposition on C-fiber textiles that had Ni and Cu catalyst deposited via electrophoretic deposition. Before the CNFs were coated with silica layer via hydrolysis of TEOS (Tetraethyl orthosilicate), the carbon nanofibers were oxidized by nitric acid. Due to oxidation, the hydroxyl group was created on the carbon nanofibers and this was used as an activation site for the SiO2. The physicochemical properties of the grown carbon nanofibers were investigated with Scanning electron microscopy (SEM), Energy dispersive spectroscopy (EDS), X-ray Diffraction (XRD), Raman spectroscopy, and X-ray photoelectron spectroscopy (XPS). The structures of SiO2-coated carbon nanofibers were characterized by XPS and TEM. The electrochemical properties and the capacitance of the materials were investigated by galvanostatic charge-discharge and cyclic voltammetry. Different types of carbon nanofibers were grown upon the deposition utilizing catalysts, with the SiO2 uniformly coated on the surface of carbon nanofibers. When used as an anode material for the Li secondary battery, the SiO2/CNFs composite had a lower capacity maintenance and a greater discharge capacity as compared to the carbon nanofibers. PMID:26726630

  14. Carbon Nanofibers (CNFs) Surface Modification to Fabricate Carbon Nanofibers_Nanopaper Integrated Polymer Composite Material.

    PubMed

    Jiang, Jianjun; Zhao, Ziwei; Deng, Chao; Liu, Fa; Li, Dejia; Fang, Liangchao; Zhang, Dan; Castro Jose M; Chen, Feng; Lee, L James

    2016-06-01

    Carbon Nanofibers (CNFs) have shown great potential to improve the physical and mechanical properties of conventional Fiber Reinforced Polymer Composites (FRPCs) surface. Excellent dispersion CNFs into water or polymer matrix was very crucial to get good quality CNFs enhanced FRPCs. Because of the hydrophobic properties of CNFs, we apply the reversible switching principles to transfer the hydrophobic surface into hydrophilic surface by growing polyaniline nanograss on the surface of CNFs which was carried out in hydrochloric acid condition. Incorporating CNFs into FRPCs as a surface layer named CNFs Nanopaper to increase the erosion resistance and electrical conductivity in this research which was very important in the wind energy field. In order to get high quality dispersed CNFs suspension, a sonication unit was used to detangle and uniform disperse the functionalized CNFs. A filter with vacuum pressure used to filter the suspension of CNFs onto Carbon veil to make CNFs Nanopaper. Vacuum Aided Resin Transfer Modeling (VARTM) process was used to fabricate Nano-enhanced FRPCs samples. In order to characterize the mechanical properties, three point bending experiment was measured. The flexural strength capacity and deformation resistance and behavior were compared and analyzed. In this paper, we discussed the methods used and provided experimental parameter and experimental results. PMID:27427606

  15. A nanobursa mesh: a graded electrospun nanofiber mesh with metal nanoparticles on carbon nanotubes

    NASA Astrophysics Data System (ADS)

    Senturk-Ozer, Semra; Chen, Tao; Degirmenbasi, Nebahat; Gevgilili, Halil; Podkolzin, Simon G.; Kalyon, Dilhan M.

    2014-07-01

    A new type of material, a ``nanobursa'' mesh (from ``bursa'' meaning ``sac or pouch''), is introduced. This material consists of sequential layers of porous polymeric nanofibers encapsulating carbon nanotubes, which are functionalized with different metal nanoparticles in each layer. The nanobursa mesh is fabricated via a novel combination of twin-screw extrusion and electrospinning. Use of this hybrid process at industrially-relevant rates is demonstrated by producing a nanobursa mesh with graded layers of Pd, Co, Ag, and Pt nanoparticles. The potential use of the fabricated nanobursa mesh is illustrated by modeling of catalytic hydrocarbon oxidation.A new type of material, a ``nanobursa'' mesh (from ``bursa'' meaning ``sac or pouch''), is introduced. This material consists of sequential layers of porous polymeric nanofibers encapsulating carbon nanotubes, which are functionalized with different metal nanoparticles in each layer. The nanobursa mesh is fabricated via a novel combination of twin-screw extrusion and electrospinning. Use of this hybrid process at industrially-relevant rates is demonstrated by producing a nanobursa mesh with graded layers of Pd, Co, Ag, and Pt nanoparticles. The potential use of the fabricated nanobursa mesh is illustrated by modeling of catalytic hydrocarbon oxidation. Electronic supplementary information (ESI) available: Experimental methods and computational details. See DOI: 10.1039/c4nr01145g

  16. Vertically Aligned Carbon Nanofiber based Biosensor Platform for Glucose Sensor

    SciTech Connect

    Al Mamun, Khandaker A.; Tulip, Fahmida S.; MacArthur, Kimberly; McFarlane, Nicole; Islam, Syed K.; Hensley, Dale

    2014-03-01

    Vertically aligned carbon nanofibers (VACNFs) have recently become an important tool for biosensor design. Carbon nanofibers (CNF) have excellent conductive and structural properties with many irregularities and defect sites in addition to exposed carboxyl groups throughout their surfaces. These properties allow a better immobilization matrix compared to carbon nanotubes and offer better resolution when compared with the FET-based biosensors. VACNFs can be deterministically grown on silicon substrates allowing optimization of the structures for various biosensor applications. Two VACNF electrode architectures have been employed in this study and a comparison of their performances has been made in terms of sensitivity, sensing limitations, dynamic range, and response time. The usage of VACNF platform as a glucose sensor has been verified in this study by selecting an optimum architecture based on the VACNF forest density. Read More: http://www.worldscientific.com/doi/abs/10.1142/S0129156414500062

  17. Synthesis of amorphous carbon nanofibers using iron nanoparticles as catalysts

    NASA Astrophysics Data System (ADS)

    Ali, Mokhtar; Ramana, G. Venkata; Padya, Balaji; Srikanth, V. V. S. S.; Jain, P. K.

    2013-06-01

    Amongst various carbon nanomaterials, carbon nanofibers (CNFs) have lately attracted considerable interest as a promising reinforcement in polymer matrix composites. CNFs are often synthesized using copper nanoparticles as catalysts and by using chemical vapor deposition (CVD). In this work iron (Fe) nanoparticles are used as catalysts to synthesize amorphous carbon nanofibers. This owes significance since Fe nanoparticles often lead to tubes rather than fibers. Fe nanoparticles (size ˜30-60nm) are prepared by first mixing an appropriate quantity of potassium sodium tartrate tetrahydrate salt with iron (II) chloride dehydrate to obtain iron tartrate and then dried and heated in vacuum oven at about 250°C to remove tartrate. In a subsequent step, CNFs are obtained by using CVD. Acetylene was used as the carbon source in the CVD process. Scanning and transmission electron microscopy show the formation of nanofibers whose diameter is dependent on the size of Fe catalysts. Raman scattering from the fibers show that they are made up of carbon and are amorphous.

  18. Hierarchical carbon nanostructure design: ultra-long carbon nanofibers decorated with carbon nanotubes

    NASA Astrophysics Data System (ADS)

    El Mel, A. A.; Achour, A.; Xu, W.; Choi, C. H.; Gautron, E.; Angleraud, B.; Granier, A.; Le Brizoual, L.; Djouadi, M. A.; Tessier, P. Y.

    2011-10-01

    Hierarchical carbon nanostructures based on ultra-long carbon nanofibers (CNF) decorated with carbon nanotubes (CNT) have been prepared using plasma processes. The nickel/carbon composite nanofibers, used as a support for the growth of CNT, were deposited on nanopatterned silicon substrate by a hybrid plasma process, combining magnetron sputtering and plasma-enhanced chemical vapor deposition (PECVD). Transmission electron microscopy revealed the presence of spherical nanoparticles randomly dispersed within the carbon nanofibers. The nickel nanoparticles have been used as a catalyst to initiate the growth of CNT by PECVD at 600 °C. After the growth of CNT onto the ultra-long CNF, SEM imaging revealed the formation of hierarchical carbon nanostructures which consist of CNF sheathed with CNTs. Furthermore, we demonstrate that reducing the growth temperature of CNT to less than 500 °C leads to the formation of carbon nanowalls on the CNF instead of CNT. This simple fabrication method allows an easy preparation of hierarchical carbon nanostructures over a large surface area, as well as a simple manipulation of such material in order to integrate it into nanodevices.

  19. Hierarchical carbon nanostructure design: ultra-long carbon nanofibers decorated with carbon nanotubes.

    PubMed

    El Mel, A A; Achour, A; Xu, W; Choi, C H; Gautron, E; Angleraud, B; Granier, A; Le Brizoual, L; Djouadi, M A; Tessier, P Y

    2011-10-28

    Hierarchical carbon nanostructures based on ultra-long carbon nanofibers (CNF) decorated with carbon nanotubes (CNT) have been prepared using plasma processes. The nickel/carbon composite nanofibers, used as a support for the growth of CNT, were deposited on nanopatterned silicon substrate by a hybrid plasma process, combining magnetron sputtering and plasma-enhanced chemical vapor deposition (PECVD). Transmission electron microscopy revealed the presence of spherical nanoparticles randomly dispersed within the carbon nanofibers. The nickel nanoparticles have been used as a catalyst to initiate the growth of CNT by PECVD at 600°C. After the growth of CNT onto the ultra-long CNF, SEM imaging revealed the formation of hierarchical carbon nanostructures which consist of CNF sheathed with CNTs. Furthermore, we demonstrate that reducing the growth temperature of CNT to less than 500°C leads to the formation of carbon nanowalls on the CNF instead of CNT. This simple fabrication method allows an easy preparation of hierarchical carbon nanostructures over a large surface area, as well as a simple manipulation of such material in order to integrate it into nanodevices. PMID:21971265

  20. Synthesis and characterization of multiwalled CNT-PAN based composite carbon nanofibers via electrospinning.

    PubMed

    Kaur, Narinder; Kumar, Vipin; Dhakate, Sanjay R

    2016-01-01

    Electrospun fibrous membranes find place in diverse applications like sensors, filters, fuel cell membranes, scaffolds for tissue engineering, organic electronics etc. The objectives of present work are to electrospun polyacrylonitrile (PAN) nanofibers and PAN-CNT nanocomposite nanofibers and convert into carbon nanofiber and carbon-CNT composite nanofiber. The work was divided into two parts, development of nanofibers and composite nanofiber. The PAN nanofibers were produced from 9 wt% PAN solution by electrospinning technique. In another case PAN-CNT composite nanofibers were developed from different concentrations of MWCNTs (1-3 wt%) in 9 wt% PAN solution by electrospinning. Both types of nanofibers were undergone through oxidation, stabilization, carbonization and graphitization. At each stage of processing of carbon and carbon-CNT composite nanofibers were characterized by SEM, AFM, TGA and XRD. It was observed that diameter of nanofiber varies with processing parameters such as applied voltage tip to collector distance, flow rate of solution and polymer concentrations etc. while in case of PAN-CNT composite nanofiber diameter decreases with increasing concentration of CNT in PAN solution. Also with stabilization, carbonization and graphitization diameter of nanofiber decreases. SEM images shows that the minimum fiber diameter in case of 3 wt% of CNT solution because as viscosity increases it reduces the phase separation of PAN and solvent and as a consequence increases in the fiber diameter. AFM images shows that surface of film is irregular which give idea about mat type orientation of fibers. XRD results show that degree of graphitization increases on increasing CNT concentration because of additional stresses exerting on the nanofiber surface in the immediate vicinity of CNTs. TGA results shows wt loss decreases as CNT concentration increases in fibers. PMID:27217998

  1. Facile Synthesis of Coaxial CNTs/MnOx-Carbon Hybrid Nanofibers and Their Greatly Enhanced Lithium Storage Performance

    NASA Astrophysics Data System (ADS)

    Yang, Zunxian; Lv, Jun; Pang, Haidong; Yan, Wenhuan; Qian, Kun; Guo, Tailiang; Guo, Zaiping

    2015-12-01

    Carbon nanotubes (CNTs)/MnOx-Carbon hybrid nanofibers have been successfully synthesized by the combination of a liquid chemical redox reaction (LCRR) and a subsequent carbonization heat treatment. The nanostructures exhibit a unique one-dimensional core/shell architecture, with one-dimensional CNTs encapsulated inside and a MnOx-carbon composite nanoparticle layer on the outside. The particular porous characteristics with many meso/micro holes/pores, the highly conductive one-dimensional CNT core, as well as the encapsulating carbon matrix on the outside of the MnOx nanoparticles, lead to excellent electrochemical performance of the electrode. The CNTs/MnOx-Carbon hybrid nanofibers exhibit a high initial reversible capacity of 762.9 mAhg-1, a high reversible specific capacity of 560.5 mAhg-1 after 100 cycles, and excellent cycling stability and rate capability, with specific capacity of 396.2 mAhg-1 when cycled at the current density of 1000 mAg-1, indicating that the CNTs/MnOx-Carbon hybrid nanofibers are a promising anode candidate for Li-ion batteries.

  2. Facile Synthesis of Coaxial CNTs/MnOx-Carbon Hybrid Nanofibers and Their Greatly Enhanced Lithium Storage Performance.

    PubMed

    Yang, Zunxian; Lv, Jun; Pang, Haidong; Yan, Wenhuan; Qian, Kun; Guo, Tailiang; Guo, Zaiping

    2015-01-01

    Carbon nanotubes (CNTs)/MnOx-Carbon hybrid nanofibers have been successfully synthesized by the combination of a liquid chemical redox reaction (LCRR) and a subsequent carbonization heat treatment. The nanostructures exhibit a unique one-dimensional core/shell architecture, with one-dimensional CNTs encapsulated inside and a MnOx-carbon composite nanoparticle layer on the outside. The particular porous characteristics with many meso/micro holes/pores, the highly conductive one-dimensional CNT core, as well as the encapsulating carbon matrix on the outside of the MnOx nanoparticles, lead to excellent electrochemical performance of the electrode. The CNTs/MnOx-Carbon hybrid nanofibers exhibit a high initial reversible capacity of 762.9 mAhg(-1), a high reversible specific capacity of 560.5 mAhg(-1) after 100 cycles, and excellent cycling stability and rate capability, with specific capacity of 396.2 mAhg(-1) when cycled at the current density of 1000 mAg(-1), indicating that the CNTs/MnOx-Carbon hybrid nanofibers are a promising anode candidate for Li-ion batteries. PMID:26621615

  3. Facile Synthesis of Coaxial CNTs/MnOx-Carbon Hybrid Nanofibers and Their Greatly Enhanced Lithium Storage Performance

    PubMed Central

    Yang, Zunxian; Lv, Jun; Pang, Haidong; Yan, Wenhuan; Qian, Kun; Guo, Tailiang; Guo, Zaiping

    2015-01-01

    Carbon nanotubes (CNTs)/MnOx-Carbon hybrid nanofibers have been successfully synthesized by the combination of a liquid chemical redox reaction (LCRR) and a subsequent carbonization heat treatment. The nanostructures exhibit a unique one-dimensional core/shell architecture, with one-dimensional CNTs encapsulated inside and a MnOx-carbon composite nanoparticle layer on the outside. The particular porous characteristics with many meso/micro holes/pores, the highly conductive one-dimensional CNT core, as well as the encapsulating carbon matrix on the outside of the MnOx nanoparticles, lead to excellent electrochemical performance of the electrode. The CNTs/MnOx-Carbon hybrid nanofibers exhibit a high initial reversible capacity of 762.9 mAhg−1, a high reversible specific capacity of 560.5 mAhg−1 after 100 cycles, and excellent cycling stability and rate capability, with specific capacity of 396.2 mAhg−1 when cycled at the current density of 1000 mAg−1, indicating that the CNTs/MnOx-Carbon hybrid nanofibers are a promising anode candidate for Li-ion batteries. PMID:26621615

  4. Direct imaging of copper catalyst migration inside helical carbon nanofibers.

    PubMed

    Dong, Lifeng; Yu, Liyan; Cui, Zuolin; Dong, Hongzhou; Ercius, Peter; Song, Chengyu; Duden, Thomas

    2012-01-27

    By using a double-aberration-corrected (scanning) transmission electron microscope (STEM/TEM) at an acceleration voltage of only 80 kV, we demonstrate that, due to the low solubility of copper (Cu) in carbon and its affinity with oxygen (O), single-crystal Cu catalysts dissociate into small cuprous oxide (Cu2O) nanoparticles after the growth of carbon nanofibers, and Cu2O nanoparticles ultimately localize on the fiber surfaces. This new finding is a step toward a better understanding of the interactions between Cu catalysts and carbon nanomaterials and could suggest a simple and effective method for eliminating Cu impurities from the fibers. PMID:22172975

  5. Template Synthesis of Carbon Nanofibers Containing Linear Mesocage Arrays

    PubMed Central

    2010-01-01

    Carbon nanofibers containing linear mesocage arrays were prepared via evaporation induced self-assembly method within AAO template with an average channel diameter of about 25 nm. The TEM results show that the mesocages have an elongated shape in the transversal direction. The results of N2 adsorption–desorption analysis indicate that the sample possesses a cage-like mesoporous structure and the average mesopore size of the sample is about 18 nm. PMID:20671793

  6. Preparation of Surface Adsorbed and Impregnated Multi-walled Carbon Nanotube/Nylon-6 Nanofiber Composites and Investigation of their Gas Sensing Ability

    PubMed Central

    Lala, Neeta L.; Thavasi, Velmurugan; Ramakrishna, Seeram

    2009-01-01

    We have prepared electrospun Nylon-6 nanofibers via electrospinning, and adsorbed multi-walled carbon nanotubes (MWCNTs) onto the surface of Nylon-6 fibers using Triton® X-100 to form a MWCNTs/Nylon-6 nanofiber composite. The dispersed MWCNTs have been found to be stable in hexafluoroisopropanol for several months without precipitation. A MWCNTs/Nylon-6 nanofiber composite based chemical sensor has demonstrated its responsiveness towards a wide range of solvent vapours at room temperature and only mg quantities of MWCNTs were expended. The large surface area and porous nature of the electrospun Nylon-6/MWCNT nanofibers facilitates greater analyte permeability. The experimental analysis has indicated that the dipole moment, functional group and vapour pressure of the analytes determine the magnitude of the responsiveness. PMID:22389589

  7. Effect of carbon nanofiber dispersion on the properties of PIP-SiC/SiC composites

    NASA Astrophysics Data System (ADS)

    Taguchi, T.; Hasegawa, Y.; Shamoto, S.

    2011-10-01

    SiC/SiC composites with and without dispersed carbon nanofiber were fabricated by the polymer impregnation and pyrolysis process. The effect of dispersing carbon nanofiber on the mechanical and thermal properties of SiC/SiC composites was investigated. The bending strength and elastic modulus of SiC/SiC composites with carbon nanofiber decreased slightly compared to those of the SiC/SiC composites without the nanofiber. On the other hand, the thermal conductivity of SiC/SiC composites increased with increasing amount of dispersed nanofiber. The dominant reason is considered to be that the pore shape changed from an oblong shape perpendicular to the direction of heat flow to an isotropic. The shape change resulted from the dispersed carbon nanofiber.

  8. Decreased functions of astrocytes on carbon nanofiber materials.

    PubMed

    McKenzie, Janice L; Waid, Michael C; Shi, Riyi; Webster, Thomas J

    2004-01-01

    Carbon nanofibers possess excellent conductivity properties, which may be beneficial in the design of more effective neural prostheses; however, limited evidence on their cytocompatibility properties currently exists. The objective of the present in vitro study was to determine cytocompatibility properties of formulations containing carbon nanofibers pertinent to neural implant applications. Substrates were prepared from four different types of carbon fibers, two with nanoscale diameters (nanophase, or less than or equal to 100 nm) and two with conventional diameters (or greater than 100 nm). Within these two categories, both a high and a low surface energy fiber were investigated and tested. Carbon fibers were compacted in a manual hydraulic press via a uniaxial loading cycle. Astrocytes (glial scar tissue-forming cells) were seeded onto the substrates for adhesion, proliferation, and long-term function studies (such as total intracellular protein and alkaline phosphatase activity). Results provided the first evidence that astrocytes preferentially adhered and proliferated on carbon fibers that had the largest diameter and the lowest surface energy. Based on these results, composite substrates were also formed using different weight percentages (0-25 wt%) of the nanophase, high surface energy fibers in a polycarbonate urethane matrix. Results provided the first evidence of decreased adhesion of astrocytes with increasing weight percents of the high surface energy carbon nanofibers in the polymer composite; this further demonstrates that formulations containing carbon fibers in the nanometer regime may limit astrocyte functions leading to decreased glial scar tissue formation. Positive interactions with neurons, and, at the same time, limited astrocyte functions leading to decreased gliotic scar tissue formation are essential for increased neuronal implant efficacy. PMID:14643605

  9. Physicochemical investigations of carbon nanofiber supported Cu / ZrO2 catalyst

    NASA Astrophysics Data System (ADS)

    Din, Israf Ud; Shaharun, Maizatul S.; Subbarao, Duvvuri; Naeem, A.

    2014-10-01

    Zirconia-promoted copper/carbon nanofiber catalysts (Cu - ZrO2/ CNF ) were prepared by the sequential deposition precipitation method. The Herringbone type of carbon nanofiber GNF-100 (Graphite nanofiber) was used as a catalyst support. Carbon nanofiber was oxidized to (CNF-O) with 5% and 65 % concentration of nitric acid (HNO3). The CNF activated with 5% HNO3 produced higher surface area which is 155 m2/g. The catalyst was characterized by X-ray Diffraction (XRD), Fourier Transform Infra-Red (FTIR) and N2 adsorption-desorption. The results showed that increase of HNO3 concentration reduced the surface area and porosity of the catalyst.

  10. Porous Carbon Nanoparticle Networks with Tunable Absorbability

    PubMed Central

    Dai, Wei; Kim, Seong Jin; Seong, Won-Kyeong; Kim, Sang Hoon; Lee, Kwang-Ryeol; Kim, Ho-Young; Moon, Myoung-Woon

    2013-01-01

    Porous carbon materials with high specific surface areas and superhydrophobicity have attracted much research interest due to their potential application in the areas of water filtration, water/oil separation, and oil-spill cleanup. Most reported superhydrophobic porous carbon materials are fabricated by complex processes involving the use of catalysts and high temperatures but with low throughput. Here, we present a facile single-step method for fabricating porous carbon nanoparticle (CNP) networks with selective absorbability for water and oils via the glow discharge of hydrocarbon plasma without a catalyst at room temperature. Porous CNP networks were grown by the continuous deposition of CNPs at a relatively high deposition pressure. By varying the fluorine content, the porous CNP networks exhibited tunable repellence against liquids with various degrees of surface tension. These porous CNP networks could be applied for the separation of not only water/oil mixtures but also mixtures of liquids with different surface tension levels. PMID:23982181

  11. Carbon nanofibers synthesized by decomposition of alcohol at atmospheric pressure

    NASA Astrophysics Data System (ADS)

    Jiang, N.; Koie, R.; Inaoka, T.; Shintani, Y.; Nishimura, K.; Hiraki, A.

    2002-07-01

    In the present study, we fabricated the carbon nanofibers (CNFs) by decomposition of methyl alcohol at atmospheric pressure. The CNFs were grown on Ni/Si substrates using simplified hot-filament chemical vapor deposition equipment. The deposits mainly consist of the semicrystalline CNFs, in which a few of carbon nanotubes are included. On the 30-nm-thick Ni/Si substrates, the mean length of the CNFs is 2-3 mum, and their average diameter is less than 100 nm. The as-deposited CNFs were evaluated by both scanning and transmission electron microscopes. The field-electron-emission properties of CNFs were characterized as well.

  12. Functionalized carbon nanotubes and nanofibers for biosensing applications

    PubMed Central

    Wang, Jun; Lin, Yuehe

    2008-01-01

    This review summarizes recent advances in electrochemical biosensors based on carbon nanotubes (CNTs) and carbon nanofibers (CNFs) with an emphasis on applications of CNTs. CNTs and CNFs have unique electric, electrocatalytic and mechanical properties, which make them efficient materials for developing electrochemical biosensors. We discuss functionalizing CNTs for biosensors. We review electrochemical biosensors based on CNTs and their various applications (e.g., measurement of small biological molecules and environmental pollutants, detection of DNA, and immunosensing of disease biomarkers). Moreover, we outline the development of electrochemical biosensors based on CNFs and their applications. Finally, we discuss some future applications of CNTs. PMID:19122842

  13. High-capacity Li2Mn0.8Fe0.2SiO4/carbon composite nanofiber cathodes for lithium-ion batteries

    NASA Astrophysics Data System (ADS)

    Zhang, Shu; Li, Ying; Xu, Guanjie; Li, Shuli; Lu, Yao; Toprakci, Ozan; Zhang, Xiangwu

    2012-09-01

    Li2MnSiO4 has been considered as a promising cathode material with an extremely high theoretically capacity of 332 mAh g-1. However, due to its low intrinsic conductivity and poor structural stability, only about half of the theoretical capacity has been realized in practice and the capacity decays rapidly during cycling. To realize the high capacity and improve the cycling performance, Li2Mn0.8Fe0.2SiO4/carbon composite nanofibers were prepared by the combination of iron doping and electrospinning. X-ray diffraction, scanning electron microscope, and transmission electronic microscope were applied to characterize the Li2Mn0.8Fe0.2SiO4/carbon nanofibers. It was found that Li2Mn0.8Fe0.2SiO4 nanoparticles were embedded into continuous carbon nanofiber matrices, which formed free-standing porous mats that could be used as binder-free cathodes. The iron doping improved the conductivity and purity of the active material, and the carbon nanofiber matrix facilitated ion transfer and charge diffusion. As a result, Li2Mn0.8Fe0.2SiO4/carbon nanofiber cathodes showed promising improvement on reversible capacity and cycling performance.

  14. Catalyst-loaded porous WO3 nanofibers using catalyst-decorated polystyrene colloid templates for detection of biomarker molecules.

    PubMed

    Choi, Seon-Jin; Kim, Sang-Joon; Koo, Won-Tae; Cho, Hee-Jin; Kim, Il-Doo

    2015-02-14

    Pore-loaded WO3 nanofibers (NFs) functionalized with spherical catalyst films were achieved via electrospinning combined by the sacrificial templating route using layer-by-layer (LbL) catalyst assembled polystyrene (PS) colloids. The catalyst-loaded porous WO3 NFs exhibited significantly improved toluene and acetone detection capability for potential application in exhaled breath analysis. PMID:25572467

  15. Occupational nanosafety considerations for carbon nanotubes and carbon nanofibers.

    PubMed

    Castranova, Vincent; Schulte, Paul A; Zumwalde, Ralph D

    2013-03-19

    Carbon nanotubes (CNTs) are carbon atoms arranged in a crystalline graphene lattice with a tubular morphology. CNTs exhibit high tensile strength, possess unique electrical properties, are durable, and can be functionalized. These properties allow applications as structural materials, in electronics, as heating elements, in batteries, in the production of stain-resistant fabric, for bone grafting and dental implants, and for targeted drug delivery. Carbon nanofibers (CNFs) are strong, flexible fibers that are currently used to produce composite materials. Agitation can lead to aerosolized CNTs and CNFs, and peak airborne particulate concentrations are associated with workplace activities such as weighing, transferring, mixing, blending, or sonication. Most airborne CNTs or CNFs found in workplaces are loose agglomerates of micrometer diameter. However, due to their low density, they linger in workplace air for a considerable time, and a large fraction of these structures are respirable. In rat and mouse models, pulmonary exposure to single-walled carbon nanotubes (SWCNTs), multi-walled carbon nanotubes (MWCNTs), or CNFs causes the following pulmonary reactions: acute pulmonary inflammation and injury, rapid and persistent formation of granulomatous lesions at deposition sites of large CNT agglomerates, and rapid and progressive alveolar interstitial fibrosis at deposition sites of more dispersed CNT or CNF structures. Pulmonary exposure to SWCNTs can induce oxidant stress in aortic tissue and increases plaque formation in an atherosclerotic mouse model. Pulmonary exposure to MWCNTs depresses the ability of coronary arterioles to respond to dilators. These cardiovascular effects may result from neurogenic signals from sensory irritant receptors in the lung. Pulmonary exposure to MWCNTs also upregulates mRNA for inflammatory mediators in selected brain regions, and pulmonary exposure to SWCNTs upregulates the baroreceptor reflex. In addition, pulmonary exposure to

  16. The effect of embedded carbon nanotubes on the morphological evolution during the carbonization of poly(acrylonitrile) nanofibers.

    PubMed

    Prilutsky, Sabina; Zussman, Eyal; Cohen, Yachin

    2008-04-23

    Hybrid nanofibers with different concentrations of multi-walled carbon nanotubes (MWCNTs) in polyacrylonitrile (PAN) were fabricated using the electrospinning technique and subsequently carbonized. The morphology of the fabricated carbon nanofibers (CNFs) at different stages of the carbonization process was characterized by transmission electron microscopy and Raman spectroscopy. The polycrystalline nature of the CNFs was shown, with increasing content of ordered crystalline regions having enhanced orientation with increasing content of MWCNTs. The results indicate that embedded MWCNTs in the PAN nanofibers nucleate the growth of carbon crystals during PAN carbonization. PMID:21825647

  17. Oxygen adsorption-induced surface segregation of titanium oxide by activation in carbon nanofibers for maximizing photocatalytic performance.

    PubMed

    Lee, Sung-In; Jo, Seong-Mu; Joh, Han-Ik; Lee, Myong-Hoon; Lee, Sungho

    2015-02-14

    This research demonstrates a simple method for synthesizing titanium dioxide nanoparticle-decorated carbon nanofibers. These nanofibers showed highly efficient degradation of methylene blue under UV light because of the synergistic effects of the large surface-active sites of titanium dioxide nanoparticles and the carbon nanofibers on the photocatalytic properties. PMID:25575123

  18. Reverse Kebab Structure Formed inside Carbon Nanofibers via Nanochannel Flow.

    PubMed

    Nie, Min; Kalyon, Dilhan M; Fisher, Frank T

    2015-09-15

    The morphology of polymers inside a confined space has raised great interest in recent years. However, polymer crystallization within a one-dimensional carbon nanostructure is challenging due to the difficulty of polar solvents carrying polymers to enter a nonpolar graphitic nanotube in bulk solution at normal temperature and pressure. Here we describe a method whereby nylon-11 was crystallized and periodically distributed on the individual graphitic nanocone structure within hollow carbon nanofibers (CNF). Differential scanning calorimetry and X-ray diffraction indicate that the nylon polymer is in the crystalline phase. A mechanism is suggested for the initiation of nanochannel flow in a bulk solvent as a prerequisite condition to achieve interior polymer crystallization. Selective etching of polymer crystals on the outer wall of CNF indicates that both surface tension and viscosity affect the flow within the CNF. This approach provides an opportunity for the interior functionalization of carbon nanotubes and nanofibers for applications in the biomedical, energy, and related fields. PMID:26313253

  19. Functionalized ultra-porous titania nanofiber membranes as nuclear waste separation and sequestration scaffolds for nuclear fuels recycle.

    SciTech Connect

    Liu, Haiqing; Bell, Nelson Simmons; Cipiti, Benjamin B.; Lewis, Tom Goslee,; Sava, Dorina Florentina; Nenoff, Tina Maria

    2012-09-01

    Advanced nuclear fuel cycle concept is interested in reducing separations to a simplified, one-step process if possible. This will benefit from the development of a one-step universal getter and sequestration material so as a simplified, universal waste form was proposed in this project. We have developed a technique combining a modified sol-gel chemistry and electrospinning for producing ultra-porous ceramic nanofiber membranes with controllable diameters and porous structures as the separation/sequestration materials. These ceramic nanofiber materials have been determined to have high porosity, permeability, loading capacity, and stability in extreme conditions. These porous fiber membranes were functionalized with silver nanoparticles and nanocrystal metal organic frameworks (MOFs) to introduce specific sites to capture gas species that are released during spent nuclear fuel reprocessing. Encapsulation into a durable waste form of ceramic composition was also demonstrated.

  20. Investigation of Lithium-Air Battery Discharge Product Formed on Carbon Nanotube and Nanofiber Electrodes

    NASA Astrophysics Data System (ADS)

    Mitchell, Robert Revell, III

    Carbon nanotubes have been actively investigated for integration in a wide variety of applications since their discovery over 20 years ago. Their myriad desirable material properties including exceptional mechanical strength, high thermal conductivities, large surface-to-volume ratios, and considerable electrical conductivities, which are attributable to a quantum mechanical ability to conduct electrons ballistically, have continued to motivate interest in this material system. While a variety of synthesis techniques exist, carbon nanotubes and nanofibers are most often conveniently synthesized using chemical vapor deposition (CVD), which involves their catalyzed growth from transition metal nanoparticles. Vertically-aligned nanotube and nanofiber carpets produced using CVD have been utilized in a variety of applications including those related to energy storage. Li-air (Li-O2) batteries have received much interest recently because of their very high theoretical energy densities (3200 Wh/kgLi2O2 ). which make them ideal candidates for energy storage devices for future fully-electric vehicles. During operation of a Li-air battery O2 is reduced on the surface a porous air cathode, reacting with Li-ions to form lithium peroxide (Li-O2). Unlike the intercalation reactions of Li-ion batteries, discharge in a Li-air cell is analogous to an electrodeposition process involving the nucleation and growth of the depositing species on a foreign substrate. Carbon nanofiber electrodes were synthesized on porous substrates using a chemical vapor deposition process and then assembled into Li-O2 cells. The large surface to volume ratio and low density of carbon nanofiber electrodes were found to yield a very high gravimetric energy density in Li-O 2 cells, approaching 75% of the theoretical energy density for Li 2O2. Further, the carbon nanofiber electrodes were found to be excellent platforms for conducting ex situ electron microscopy investigations of the deposition Li2O2 phase

  1. One-Pot Synthesis of Carbon Nanofibers from CO2.

    PubMed

    Ren, Jiawen; Li, Fang-Fang; Lau, Jason; González-Urbina, Luis; Licht, Stuart

    2015-09-01

    Carbon nanofibers, CNFs, due to their superior strength, conductivity, flexibility, and durability have great potential as a material resource but still have limited use due to the cost intensive complexities of their synthesis. Herein, we report the high-yield and scalable electrolytic conversion of atmospheric CO2 dissolved in molten carbonates into CNFs. It is demonstrated that the conversion of CO2 → CCNF + O2 can be driven by efficient solar, as well as conventional, energy at inexpensive steel or nickel electrodes. The structure is tuned by controlling the electrolysis conditions, such as the addition of trace transition metals to act as CNF nucleation sites, the addition of zinc as an initiator and the control of current density. A less expensive source of CNFs will facilitate its adoption as a societal resource, and using carbon dioxide as a reactant to generate a value added product such as CNFs provides impetus to consume this greenhouse gas to mitigate climate change. PMID:26237131

  2. Fabrication and characterization of carbon nanofiber@mesoporous carbon core-shell composite for the Li-air battery

    NASA Astrophysics Data System (ADS)

    Song, Myeong Jun; Shin, Moo Whan

    2014-11-01

    In this study, we successfully design and synthesize the mesoporous carbon coated carbon nanofibers (CNF@mesoCs) for the Li-air battery. The composites are fabricated via electrospinning technique and nanocasting strategy. After mesoporous carbon coating process, the composites have retained their original one-dimensional structure as pristine carbon nanofibers. Every nanofiber entangles with each other to form a three-dimensional cross-linked web structure. Because of the mesoporous carbon coating on carbon nanofibers, the surface area increases from 708 m2 g-1 to 2194 m2 g-1. We confirm that the mesoporous carbon coated on carbon nanofibers is well-graphitized by analysis of Raman spectra. The graphitized surface of CNF@mesoCs (4.638 S cm-1) is believed to result in their higher electrical conductivity than that of pristine carbon nanofibers (3.0759 S cm-1). Without employment of any binders and metal foams, the cathode of CNF@mesoCs exhibits high discharge capacity of 4000 mA h g-1, which is much higher than that from pristine carbon nanofibers (2750 mA h g-1). This work demonstrates that the fabricated CNF@mesoCs structures have a great potential to be employed as light-weight and efficient electrode for energy storage and conversion devices.

  3. Faulting in porous carbonate grainstones

    NASA Astrophysics Data System (ADS)

    Tondi, Emanuele; Agosta, Fabrizio

    2010-05-01

    In the recent past, a new faulting mechanism has been documented within porous carbonate grainstones. This mechanism is due to strain localization into narrow tabular bands characterized by both volumetric and shear strain; for this reason, these features are named compactive shear bands. In the field, compactive shear bands are easily recognizable because they are lightly coloured with respect to the parent rock, and/or show a positive relief because of their increased resistance to weathering. Both characteristics, light colours and positive relief, are a consequence of the compaction processes that characterize these bands, which are the simplest structure element that form within porous carbonate grainstones. With ongoing deformation, the single compactive shear bands, which solve only a few mm of displacement, may evolve into zone of compactive shear bands and, finally, into well-developed faults characterized by slip surfaces and fault rocks. Field analysis conducted in key areas of Italy allow us to documented different modalities of interaction and linkage among the compactive shear bands: (i) a simple divergence of two different compactive shear bands from an original one, (ii) extensional and contractional jogs formed by two continuous, interacting compactive shear bands, and (iii) eye structures formed by collinear interacting compactive shear bands, which have been already described for deformation bands in sandstones. The last two types of interaction may localize the formation of compaction bands, which are characterized by pronounced component of compaction and negligible components of shearing, and/or pressure solution seams. All the aforementioned types of interaction and linkage could happen at any deformation stage, single bands, zone of bands or well developed faults. The transition from one deformation process to another, which is likely to be controlled by the changes in the material properties, is recorded by different ratios and

  4. A novel carbon fiber based porous carbon monolith

    SciTech Connect

    Burchell, T.D.; Klett, J.W.; Weaver, C.E.

    1995-06-01

    A novel porous carbon material based on carbon fibers has been developed. The material, when activated, develops a significant micro- or mesopore volume dependent upon the carbon fiber type utilized (isotropic pitch or polyacrylonitrile). The materials will find applications in the field of fluid separations or as a catalyst support. Here, the manufacture and characterization of our porous carbon monoliths are described. A novel adsorbent carbon composite material has been developed comprising carbon fibers and a binder. The material, called carbon fiber composite molecular sieve (CFCMS), was developed through a joint research program between Oak Ridge National Laboratory (ORNL) and the University of Kentucky, Center for Applied Energy Research (UKCAER).

  5. A comparative study of EMI shielding properties of carbon nanofiber and multi-walled carbon nanotube filled polymer composites.

    PubMed

    Yang, Yonglai; Gupta, Mool C; Dudley, Kenneth L; Lawrence, Roland W

    2005-06-01

    Electromagnetic interference shielding properties of carbon nanofiber- and multi-walled carbon nanotube-filled polystyrene composites were investigated in the frequency range of 8.2-12.4 GHz (X-band). It was observed that the shielding effectiveness of composites was frequency independent, and increased with the increase of carbon nanofiber or nanotube loading. At the same filler loading, multi-walled carbon nanotube-filled polystyrene composites exhibited higher shielding effectiveness compared to those filled with carbon nanofibers. In particular, carbon nanotubes were more effective than nanofibers in providing high EMI shielding at low filler loadings. The experimental data showed that the shielding effectiveness of the composite containing 7 wt% carbon nanotubes could reach more than 26 dB, implying that such a composite can be used as a potential electromagnetic interference shielding material. The dominant shielding mechanism of carbon nanotube-filled polystyrene composites was also discussed. PMID:16060155

  6. Thermal conductivity of tubrostratic carbon nanofiber networks

    DOE PAGESBeta

    Bauer, Matthew L.; Saltonstall, Chris B.; Leseman, Zayd C.; Beechem, Thomas E.; Hopkins, Patrick E.; Norris, Pamela M.

    2016-01-01

    Composite material systems composed of a matrix of nano materials can achieve combinations of mechanical and thermophysical properties outside the range of traditional systems. While many reports have studied the intrinsic thermal properties of individual carbon fibers, to be useful in applications in which thermal stability is critical, an understanding of heat transport in composite materials is required. In this work, air/ carbon nano fiber networks are studied to elucidate the system parameters influencing thermal transport. Sample thermal properties are measured with varying initial carbon fiber fill fraction, environment pressure, loading pressure, and heat treatment temperature through a bidirectional modificationmore » of the 3ω technique. The nanostructures of the individual fibers are characterized with small angle x-ray scattering and Raman spectroscopy providing insight to individual fiber thermal conductivity. Measured thermal conductivity varied from 0.010 W/(m K) to 0.070 W/(m K). An understanding of the intrinsic properties of the individual fibers and the interactions of the two phase composite is used to reconcile low measured thermal conductivities with predictive modeling. This methodology can be more generally applied to a wide range of fiber composite materials and their applications.« less

  7. Thermal conductivity of tubrostratic carbon nanofiber networks

    SciTech Connect

    Bauer, Matthew L.; Saltonstall, Chris B.; Leseman, Zayd C.; Beechem, Thomas E.; Hopkins, Patrick E.; Norris, Pamela M.

    2016-01-01

    Composite material systems composed of a matrix of nano materials can achieve combinations of mechanical and thermophysical properties outside the range of traditional systems. While many reports have studied the intrinsic thermal properties of individual carbon fibers, to be useful in applications in which thermal stability is critical, an understanding of heat transport in composite materials is required. In this work, air/ carbon nano fiber networks are studied to elucidate the system parameters influencing thermal transport. Sample thermal properties are measured with varying initial carbon fiber fill fraction, environment pressure, loading pressure, and heat treatment temperature through a bidirectional modification of the 3ω technique. The nanostructures of the individual fibers are characterized with small angle x-ray scattering and Raman spectroscopy providing insight to individual fiber thermal conductivity. Measured thermal conductivity varied from 0.010 W/(m K) to 0.070 W/(m K). An understanding of the intrinsic properties of the individual fibers and the interactions of the two phase composite is used to reconcile low measured thermal conductivities with predictive modeling. This methodology can be more generally applied to a wide range of fiber composite materials and their applications.

  8. Carbon nanofiber polymer composites: evaluation of life cycle energy use.

    PubMed

    Khanna, Vikas; Bakshi, Bhavik R

    2009-03-15

    Holistic evaluation of emerging nanotechnologies using systems analysis is pivotal for guiding their safe and sustainable development. While toxicity studies of engineered nanomaterials are essential, understanding of the potential large scale impacts of nanotechnology is also critical for developing sustainable nanoproducts. This work evaluates the life cycle energetic impact associated with the production and use of carbon nanofiber (CNF) reinforced polymer nanocomposites (PNC). Specifically, both simple CNF and carbon nanofiber-glass fiber (CNF-GF) hybrid PNCs are evaluated and compared with steel for equal stiffness design. Life cycle inventory is developed based on published literature and best available engineering information. A cradle-to-gate comparison suggests that for equal stiffness design, CNF reinforced PNCs are 1.6-12 times more energy intensive than steel. It is anticipated that the product use phase may strongly influence whether any net savings in life cycle energy consumption can be realized. A case study involving the use of CNF and CNF-GF reinforced PNCs in the body panels of automobiles highlights that the use of PNCs with lower CNF loading ratios has the potential for net life cycle energy savings relative to steel owing to improved fuel economy benefits. Other factors such as cost, toxicity impact of CNF, and end-of-life issues specific to CNFs need to be considered to evaluate the final economic and environmental performance of CNF reinforced PNC materials. PMID:19368217

  9. Chlorine effect on the formation of carbon nanofibers.

    PubMed

    Lin, Wang-Hua; Takahashi, Yusuke; Li, Yuan-Yao; Sakoda, Akiyoshi

    2012-12-01

    Platelet graphite nanofibers (GNFs) and turbostratic carbon nanofibers (CNFs) are synthesized by the thermal evaporation and decomposition of a polymer-based mixture at 700 degrees C using Ni as a catalyst. The mixture consists of poly(ethylene glycol) (PEG), serving as the carbon source, and hydrochloric acid solution (HCl(aq)), serving as the promoter/additive for the growth of CNFs. High-purity zigzag-shaped platelet GNFs form with 10 wt% HCl(aq) as an additive in the PEG. The diameters of the platelet GNFs are in the range of 40-60 nm, with lengths of a few micrometers. High-resolution transmission electron microscopy images indicate a high degree of graphitization and well ordered graphene layers along the fiber axis. In contrast, high-purity turbostratic CNFs form with 20 wt% HCl(aq) in the PEG. The diameter and length of the turbostratic CNFs are 20-40 nm and a few micrometers, respectively. The participation of HCl in the thermal process leads to the formation of Ni-Cl compounds. The amount of chlorine affects the shape of the Ni catalyst, which determines the type of CNF formed. PMID:23447943

  10. Carbon nanofibers derived from cellulose nanofibers as a long-life anode material for rechargeable sodium-ion batteries

    SciTech Connect

    Luo, W; Schardt, J; Bommier, C; Wang, B; Razink, J; Simonsen, J; Ji, XL

    2013-01-01

    A highly reversible anode is indispensable to the future success of sodium-ion batteries (SIBs). Herein, carbon nanofibers (CNFs) derived from cellulose nanofibers are investigated as an anode material for SIBs. The CNFs exhibit very promising electrochemical properties, including a high reversible capacity (255 mA h g(-1) at 40 mA g(-1)), good rate capability (85 mA h g(-1) at 2000 mA g(-1)), and excellent cycling stability (176 mA h g(-1) at 200 mA g(-1) over 600 cycles).

  11. High performance carbon nanotube - polymer nanofiber hybrid fabrics

    NASA Astrophysics Data System (ADS)

    Yildiz, Ozkan; Stano, Kelly; Faraji, Shaghayegh; Stone, Corinne; Willis, Colin; Zhang, Xiangwu; Jur, Jesse S.; Bradford, Philip D.

    2015-10-01

    Stable nanoscale hybrid fabrics containing both polymer nanofibers and separate and distinct carbon nanotubes (CNTs) are highly desirable but very challenging to produce. Here, we report the first instance of such a hybrid fabric, which can be easily tailored to contain 0-100% millimeter long CNTs. The novel CNT - polymer hybrid nonwoven fabrics were created by simultaneously electrospinning nanofibers onto aligned CNT sheets which were drawn and collected on a grounded, rotating mandrel. Due to the unique properties of the CNTs, the hybrids show very high tensile strength, very small pore size, high specific surface area and electrical conductivity. In order to further examine the hybrid fabric properties, they were consolidated under pressure, and also calendered at 70 °C. After calendering, the fabric's strength increased by an order of magnitude due to increased interactions and intermingling with the CNTs. The hybrids are highly efficient as aerosol filters; consolidated hybrid fabrics with a thickness of 20 microns and areal density of only 8 g m-2 exhibited ultra low particulate (ULPA) filter performance. The flexibility of this nanofabrication method allows for the use of many different polymer systems which provides the opportunity for engineering a wide range of nanoscale hybrid materials with desired functionalities.Stable nanoscale hybrid fabrics containing both polymer nanofibers and separate and distinct carbon nanotubes (CNTs) are highly desirable but very challenging to produce. Here, we report the first instance of such a hybrid fabric, which can be easily tailored to contain 0-100% millimeter long CNTs. The novel CNT - polymer hybrid nonwoven fabrics were created by simultaneously electrospinning nanofibers onto aligned CNT sheets which were drawn and collected on a grounded, rotating mandrel. Due to the unique properties of the CNTs, the hybrids show very high tensile strength, very small pore size, high specific surface area and electrical

  12. Method for production of polymer and carbon nanofibers from water-soluble polymers.

    PubMed

    Spender, Jonathan; Demers, Alexander L; Xie, Xinfeng; Cline, Amos E; Earle, M Alden; Ellis, Lucas D; Neivandt, David J

    2012-07-11

    Nanometer scale carbon fibers (carbon nanofibers) are of great interest to scientists and engineers in fields such as materials science, composite production, and energy storage due to their unique chemical, physical, and mechanical properties. Precursors currently used for production of carbon nanofibers are primarily from nonrenewable resources. Lignin is a renewable natural polymer existing in all high-level plants that is a byproduct of the papermaking process and a potential feedstock for carbon nanofiber production. The work presented here demonstrates a process involving the rapid freezing of an aqueous lignin solution, followed by sublimation of the resultant ice, to form a uniform network comprised of individual interconnected lignin nanofibers. Carbonization of the lignin nanofibers yields a similarly structured carbon nanofiber network. The methodology is not specific to lignin; nanofibers of other water-soluble polymers have been successfully produced. This nanoscale fibrous morphology has not been observed in traditional cryogel processes, due to the relatively slower freezing rates employed compared to those achieved in this study. PMID:22716198

  13. Effects of Microstructure of Carbon Nanofibers for Amperometric Detection of Hydrogen Peroxide

    SciTech Connect

    Li, Zhizhou; Cui, Xiaoli; Zheng, Junsheng; Wang, Qingfei; Lin, Yuehe

    2007-08-10

    Carbon nanofibers (CNFs) with different microstructures, including platelet-carbon nanofibers (PCNFs), fish-bone-carbon nanofibers (FCNFs), and tube-carbon nanofibers (TCNFs), were synthesized, characterized, and evaluated for electrochemical sensing of hydrogen peroxide. The CNFs studied here can show several microstructures in which various stacked morphologies and their sizes and graphite-layer ordering can be well controlled. Glassy carbon (GC) electrodes modified by CNFs were fabricated and compared for amperometric detection of hydrogen peroxide. Sensors of PCNFs/GC, FCNFs/GC, and TCNFs/GC were used in the amperometric detection of H2O2 in a solution of 0.05 M phosphate buffered saline solution (pH 7.4).

  14. Thermal Expansion of Carbon Nanofiber-Reinforced Multiscale Polymer Composites

    NASA Astrophysics Data System (ADS)

    Poveda, Ronald L.; Achar, Sriniket; Gupta, Nikhil

    2012-10-01

    Improved dimensional stability of composites is desired in applications where they are exposed to varying temperature conditions. The current study aims at analyzing the effect of vapor-grown carbon nanofibers (CNFs) on the thermal expansion behavior of epoxy matrix composites and hollow particle-filled composites (syntactic foams). CNFs have a lower coefficient of thermal expansion (CTE) than epoxy resin, which results in composites with increased dimensional stability as the CNF content is increased. The experimental measurements show that with 10 wt.% CNF, the composite has about 11.6% lower CTE than the matrix resin. In CNF-reinforced syntactic foams, the CTE of the composite decreases with increasing wall thickness and volume fraction of hollow particle inclusions. With respect to neat epoxy resin, a maximum decrease of 38.4% is also observed in the CNF/syntactic foams with microballoon inclusions that range from 15 vol.% to 50 vol.% in all composite mixtures. The experimental results for CNF/syntactic foam are in agreement with a modified version of Kerner's model. A combination of hollow microparticles and nanofibers has resulted in the ability to tailor the thermal expansion of the composite over a wide range.

  15. Imaging, Spectroscopy, Mechanical, Alignment and Biocompatibility Studies of Electrospun Medical Grade Polyurethane (Carbothane™ 3575A) Nanofibers and Composite Nanofibers Containing Multiwalled Carbon Nanotubes

    PubMed Central

    Sheikh, Faheem A.; Macossay, Javier; Cantu, Travis; Zhang, Xujun; Hassan, M. Shamshi; Salinas, M. Esther; Farhangi, Chakavak S.; Ahmad, Hassan; Kim, Hern; Bowlin, Gary L.

    2014-01-01

    In the present study, we discuss the electrospinning of medical grade polyurethane (Carbothane™ 3575A) nanofibers containing multi-walled-carbon-nanotubes (MWCNTs). A simple method that does not depend on additional foreign chemicals has been employed to disperse MWCNTs through high intensity sonication. Typically, a polymer solution consisting of polymer/MWCNTs has been electrospun to form nanofibers. Physiochemical aspects of prepared nanofibers were evaluated by SEM, TEM, FT-IR and Raman spectroscopy, confirming nanofibers containing MWCNTs. The biocompatibility and cell attachment of the produced nanofiber mats were investigated while culturing them in the presence of NIH 3T3 fibroblasts. The results from these tests indicated non-toxic behavior of the prepared nanofiber mats and had a significant attachment of cells towards nanofibers. The incorporation of MWCNTs into polymeric nanofibers led to an improvement in tensile stress from 11.40 ± 0.9 to 51.25 ± 5.5 MPa. Furthermore, complete alignment of the nanofibers resulted in an enhancement on tensile stress to 72.78 ± 5.5 MPa. Displaying these attributes of high mechanical properties and non-toxic nature of nanofibers are recommended for an ideal candidate for future tendon and ligament grafts. PMID:25460415

  16. Microfluidic Immuno-Biochip for Detection of Breast Cancer Biomarkers Using Hierarchical Composite of Porous Graphene and Titanium Dioxide Nanofibers.

    PubMed

    Ali, Md Azahar; Mondal, Kunal; Jiao, Yueyi; Oren, Seval; Xu, Zhen; Sharma, Ashutosh; Dong, Liang

    2016-08-17

    We report on a label-free microfluidic immunosensor with femtomolar sensitivity and high selectivity for early detection of epidermal growth factor receptor 2 (EGFR2 or ErbB2) proteins. This sensor utilizes a uniquely structured immunoelectrode made of porous hierarchical graphene foam (GF) modified with electrospun carbon-doped titanium dioxide nanofibers (nTiO2) as an electrochemical working electrode. Due to excellent biocompatibility, intrinsic surface defects, high reaction kinetics, and good stability for proteins, anatase nTiO2 are ideal for electrochemical sensor applications. The three-dimensional and porous features of GF allow nTiO2 to penetrate and attach to the surface of the GF by physical adsorption. Combining GF with functional nTiO2 yields high charge transfer resistance, large surface area, and porous access to the sensing surface by the analyte, resulting in new possibilities for the development of electrochemical immunosensors. Here, the enabling of EDC-NHS chemistry covalently immobilized the antibody of ErbB2 (anti-ErbB2) on the GF-nTiO2 composite. To obtain a compact sensor architecture, the composite working electrode was designed to hang above the gold counter electrode in a microfluidic channel. The sensor underwent differential pulse voltammetry and electrochemical impedance spectroscopy to quantify breast cancer biomarkers. The two methods had high sensitivities of 0.585 μA μM(-1) cm(-2) and 43.7 kΩ μM(-1) cm(-2) in a wide concentration range of target ErbB2 antigen from 1 × 10(-15) M (1.0 fM) to 0.1 × 10(-6) M (0.1 μM) and from 1 × 10(-13) M (0.1 pM) to 0.1 × 10(-6) M (0.1 μM), respectively. Utilization of the specific recognition element, i.e., anti-ErbB2, results in high specificity, even in the presence of identical members of the EGFR family of receptor tyrosine kinases, such as ErbB3 and ErbB4. Many promising applications in the field of electrochemical detection of chemical and biological species will derive from the

  17. Synthesis and Characterization of Carbon Nanofibers on Transition Metal Catalysts by Chemical Vapor Deposition.

    PubMed

    Hyun, Yura; Park, Eun-Sil; Mees, Karina; Park, Ho-Seon; Willert-Porada, Monika; Lee, Chang-Seop

    2015-09-01

    Carbon nanofibers were synthesized on transition metal (Fe, Co, Cu) catalysts by Chemical Vapor Deposition (CVD). The variations of thickness and surface of the fibers were investigated according to the concentration of the transition metal. In order to prepare the metal catalysts for synthesis, transition metal nitrate and copper nitrate at a weight ratio were dissolved in distilled water. The obtained catalyst precipitates were filtered and then dried for more than 24 hours at 110 degrees C. Carbon nanofibers were synthesized by using ethylene gas of carbon source by CVD after pulverization of the fully-dried catalyst precipitates. They were characterized by SEM, EDS, Raman, XRD, XPS and TG/DTA, and their specific surface area was measured by BET. The characteristics of the synthesized carbon nanofibers were greatly influenced by the concentration ratio of the metal catalysts. Especially, uniform carbon nanofibers grew when the concentration ratio of Fe and Cu was 7:3, and that of Co and Cu was 6:4. Carbon nanofibers synthesized under such concentration conditions had the best crystallizability, compared to carbon nanofibers synthesized with metal catalysts of different concentration ratios, and revealed high amorphicity as well as high specific surface area. PMID:26716326

  18. Cu-Ni composition gradient for the catalytic synthesis of vertically aligned carbon nanofibers

    SciTech Connect

    Klein, Kate L; Melechko, Anatoli Vasilievich; Rack, Philip D; Fowlkes, Jason Davidson; Meyer III, Harry M; Simpson, Michael L

    2005-01-01

    The influence of catalyst alloy composition on the growth of vertically aligned carbon nanofibers was studied using Cu-Ni thin films. Metals were co-sputtered onto a substrate to form a thin film alloy with a wide compositional gradient, as determined by Auger analysis. Carbon nanofibers were then grown from the gradient catalyst film by plasma enhanced chemical vapor deposition. The alloy composition produced substantial differences in the resulting nanofibers, which varied from branched structures at 81%Ni-19%Cu to high aspect ratio nanocones at 80%Cu-20%Ni. Electron microscopy and spectroscopy techniques also revealed segregation of the initial alloy catalyst particles at certain concentrations.

  19. Vertically aligned carbon nanofiber nanoelectrode arrays: electrochemical etching and electrode reusability

    PubMed Central

    Gupta, Rakesh K.; Meyyappan, M.; Koehne, Jessica E.

    2014-01-01

    Vertically aligned carbon nanofibers in the form of nanoelectrode arrays were grown on nine individual electrodes, arranged in a 3 × 3 array geometry, in a 2.5 cm2 chip. Electrochemical etching of the carbon nanofibers was employed for electrode activation and enhancing the electrode kinetics. Here, we report the effects of electrochemical etching on the fiber height and electrochemical properties. Electrode regeneration by amide hydrolysis and electrochemical etching is also investigated for electrode reusability. PMID:25089188

  20. Lithium intercalation in porous carbon anodes

    SciTech Connect

    Tran, T.D.; Pekala, R.W.; Mayer, S.T.

    1994-11-23

    Carbon foams derived from the phase separation of polyacrylonitrile/solvent mixtures were investigated as lithium intercalation anodes for rechargeable lithium-ion batteries. The carbon foams have a bulk density of 0.35--0.5 g/cm{sup 3}, low surface area (< 50 m{sup 2}/g), and an average cell size of 5--10 {mu}m. Polyacrylonitrile-based carbon foams doped with phosphoric acid had capacity as high as 450 mAh/g. Carbon capacity increased with increasing phosphoric acid concentration in the doping solution. The doped porous carbon anodes exhibited good cyclability and excellent coulombic efficiency.

  1. Characterization of Plasma Synthesized Vertical Carbon Nanofibers for Nanoelectronics Applications

    NASA Technical Reports Server (NTRS)

    Lee, Jaesung; Feng, Philip X.-L.; Kaul, Anupama B.

    2013-01-01

    We report on the material characterization of carbon nanofibers (CNFs) which are assembled into a three-dimensional (3D) configuration for making new nanoelectromechanical systems (NEMS). High-resolution scanning electron microscopy (SEM) and x-ray electron dispersive spectroscopy (XEDS) are employed to decipher the morphology and chemical compositions of the CNFs at various locations along individual CNFs grown on silicon (Si) and refractory nitride (NbTiN) substrates, respectively. The measured characteristics suggest interesting properties of the CNF bodies and their capping catalyst nanoparticles, and growth mechanisms on the two substrates. Laser irradiation on the CNFs seems to cause thermal oxidation and melting of catalyst nanoparticles. The structural morphology and chemical compositions of the CNFs revealed in this study should aid in the applications of the CNFs to nanoelectronics and NEMS.

  2. Electron gun using carbon-nanofiber field emitter

    NASA Astrophysics Data System (ADS)

    Sakai, Y.; Haga, A.; Sugita, S.; Kita, S.; Tanaka, S.-I.; Okuyama, F.; Kobayashi, N.

    2007-01-01

    An electron gun constructed using carbon-nanofiber (CNF) emitters and an electrostatic Einzel lens system has been characterized for the development of a high-resolution x-ray source. The CNFs used were grown on tungsten and palladium tips by plasma-enhanced chemical-vapor deposition. Electron beams with the energies of 10

  3. Electron gun using carbon-nanofiber field emitter

    SciTech Connect

    Sakai, Y.; Haga, A.; Sugita, S.; Kita, S.; Tanaka, S.-I.; Okuyama, F.; Kobayashi, N.

    2007-01-15

    An electron gun constructed using carbon-nanofiber (CNF) emitters and an electrostatic Einzel lens system has been characterized for the development of a high-resolution x-ray source. The CNFs used were grown on tungsten and palladium tips by plasma-enhanced chemical-vapor deposition. Electron beams with the energies of 10

  4. Fabrication and Characterization of Carbon Nanofiber Reinforced Shape Memory Epoxy (CNFR-SME) Composites

    NASA Astrophysics Data System (ADS)

    Wang, Jiuyang

    Shape memory polymers have a wide range of applications due to their ability to mechanically change shapes upon external stimulus, while their achievable composite counterparts prove even more versatile. An overview of literature on shape memory materials, fillers and composites was provided to pave a foundation for the materials used in the current study and their inherent benefits. This study details carbon nanofiber and composite fabrication and contrasts their material properties. In the first section, the morphology and surface chemistry of electrospun-poly(acrylonitrile)-based carbon nanofiber webs were tailored through various fabrication methods and impregnated with a shape memory epoxy. The morphologies, chemical compositions, thermal stabilities and electrical resistivities of the carbon nanofibers and composites were then characterized. In the second section, an overview of thermal, mechanical and shape memory characterization techniques for shape memory polymers and their composites was provided. Thermal and mechanical properties in addition to the kinetic and dynamic shape memory performances of neat epoxy and carbon nanofiber/epoxy composites were characterized. The various carbon nanofiber web modifications proved to have notable influence on their respective composite performances. The results from these two sections lead to an enhanced understanding of these carbon nanofiber reinforced shape memory epoxy composites and provided insight for future studies to tune these composites at will.

  5. Anodes for glucose fuel cells made of carbonized nanofibers with embedded carbon nanotubes

    NASA Astrophysics Data System (ADS)

    Prilutsky, Sabina; Cohen, Yachin; Zussman, Eyal; Makarov, Vadim; Bubis, Eugenia; Schechner, Pinchas

    2010-03-01

    Electrodes made of carbonized polyacrylonitryle nanofibers, with and without embedded multiwall carbon nanotubes (MWCNT) were fabricated by the electrospinning (ES) process and evaluated as anodes in a glucose fuel cell (FC). The effect of several processing and structural characteristics, such as the presence of MWCNTs, polymer concentration in the ES solution and silver electroless plating, on FC performance were measured The carbon electrodes were successful as anodes showing significant activity even without additional silver catalyst, with noticeable improvement by incorporation of MWCNTs. The orientation of graphitic layers along the fiber axis and the coherence of layer packing were shown to be important for enhanced electrode activity. The maximal values of open circuit voltage (OCV) and peak of power density (PPD) of unmetallized electrodes, 0.4 V and 30 μW/cm^2, were found for composite carbon nanofiber electrode. Electroless silver metallization leads to enhanced performance. Maximal values of OCV and PPD of silvered electrodes were measured to be about 0.9 V and 400 μW/cm^2. Thus, carbonized nanofibers with embedded MWCNTs may form a good basis for glucose FC anodes, but better metallization and cell-configuration allowing proper mixing are required.

  6. Carbon Nanofiber/3D Nanoporous Silicon Hybrids as High Capacity Lithium Storage Materials.

    PubMed

    Park, Hyeong-Il; Sohn, Myungbeom; Kim, Dae Sik; Park, Cheolho; Choi, Jeong-Hee; Kim, Hansu

    2016-04-21

    Carbon nanofiber (CNF)/3D nanoporous (3DNP) Si hybrid materials were prepared by chemical etching of melt-spun Si/Al-Cu-Fe alloy nanocomposites, followed by carbonization using a pitch. CNFs were successfully grown on the surface of 3DNP Si particles using residual Fe impurities after acidic etching, which acted as a catalyst for the growth of CNFs. The resulting CNF/3DNP Si hybrid materials showed an enhanced cycle performance up to 100 cycles compared to that of the pristine Si/Al-Cu-Fe alloy nanocomposite as well as that of bare 3DNP Si particles. These results indicate that CNFs and the carbon coating layer have a beneficial effect on the capacity retention characteristics of 3DNP Si particles by providing continuous electron-conduction pathways in the electrode during cycling. The approach presented here provides another way to improve the electrochemical performances of porous Si-based high capacity anode materials for lithium-ion batteries. PMID:26970098

  7. Physicochemical investigations of carbon nanofiber supported Cu/ZrO{sub 2} catalyst

    SciTech Connect

    Din, Israf Ud E-mail: maizats@petronas.com.my; Shaharun, Maizatul S. E-mail: maizats@petronas.com.my; Subbarao, Duvvuri; Naeem, A.

    2014-10-24

    Zirconia-promoted copper/carbon nanofiber catalysts (Cu‐ZrO{sub 2}/CNF) were prepared by the sequential deposition precipitation method. The Herringbone type of carbon nanofiber GNF-100 (Graphite nanofiber) was used as a catalyst support. Carbon nanofiber was oxidized to (CNF-O) with 5% and 65 % concentration of nitric acid (HNO{sub 3}). The CNF activated with 5% HNO{sub 3} produced higher surface area which is 155 m{sup 2}/g. The catalyst was characterized by X-ray Diffraction (XRD), Fourier Transform Infra-Red (FTIR) and N{sub 2} adsorption-desorption. The results showed that increase of HNO{sub 3} concentration reduced the surface area and porosity of the catalyst.

  8. Neural adhesion, growth, and activity on carbon nanotubes and carbonized nanofibers

    NASA Astrophysics Data System (ADS)

    Franca, Eric William

    This dissertation focuses on how the physical and electrical properties of carbon nanotubes (CNTs) and carbonized nanofibers (CNFs) affect the physiological and electrophysiological properties of neurons and neural networks and how this may affect the efficacy of these nanomaterials as microelectrode materials. In general, the pursuit of increasing electrode sensitivity while maintaining low noise levels is addressed by investigating and utilizing novel electrode materials. Carbon nanomaterials have a native conductivity and nano-scale roughness that should decrease microelectrode noise levels and impedance by virtue of a substantially increased surface area. In addition to the beneficial microelectrode properties, these carbon nanomaterials could increase the integration of the electrode to the neural tissue. The work here is an investigation of how selected CNT and CNF materials affect the viability, outgrowth, and adhesion of cortical neurons in vitro and how the physical and chemical properties of each substrate correlates to these measurements. The intent is that properties detailed in vitro can be assumed to extrapolate to performance in vivo assuming the same materials are utilized for invasive, implanted microelectrodes. Carbon nanotubes were deposited by a layer-by-layer (LBL) method with poly(ethylenimine) (PEI). Carbon nanofiber substrates were prepared in conjunction with collaborators via electrospinning a photosensitive polymer (SU-8), photopatterning, and pyrolyzing the depositions. In addition to these substrates, control samples were prepared in the form of PEI-treated glass coverslips, carbonized thin films, SU-8 thin films, and SU-8 nanofibers. The primary variable between all of these substrates is the roughness or topography of each deposition (ranging from 0.26 nm to 160 nm average roughness). Physical and chemical characteristics of the depositions are presented in addition to the electrical characteristics which make them attractive as

  9. Zinc oxide nanorod assisted rapid single-step process for the conversion of electrospun poly(acrylonitrile) nanofibers to carbon nanofibers with a high graphitic content

    NASA Astrophysics Data System (ADS)

    Nain, Ratyakshi; Singh, Dhirendra; Jassal, Manjeet; Agrawal, Ashwini K.

    2016-02-01

    The effect of incorporation of rigid zinc oxide (ZnO) nanostructures on carbonization behavior of electrospun special acrylic fiber grade poly(acrylonitrile) (PAN-SAF) nanofibers was investigated. ZnO nanorods with high aspect ratios were incorporated into a PAN-N,N-dimethylformamide system and the composite nanofibers reinforced with aligned ZnO rods up to 50 wt% were successfully electrospun, and subsequently, carbonized. The morphology and the structural analysis of the resultant carbon nanofibers revealed that the rigid ZnO nanorods, present inside the nanofibers, possibly acted as scaffolds (temporary support structures) for immobilization of polymer chains and assisted in uniform heat distribution. This facilitated rapid and efficient conversion of the polymer structure to the ladder, and subsequently, the graphitized structure. At the end of the process, the ZnO nanorods were found to completely separate from the carbonized fibers yielding pure carbon nanofibers with a high graphitic content and surface area. The approach could be used to eliminate the slow, energy intensive stabilization step and achieve fast conversion of randomly laid carbon nanofiber webs in a single step to carbon nanofibers without the application of external tension or internal templates usually employed to achieve a high graphitic content in such systems.The effect of incorporation of rigid zinc oxide (ZnO) nanostructures on carbonization behavior of electrospun special acrylic fiber grade poly(acrylonitrile) (PAN-SAF) nanofibers was investigated. ZnO nanorods with high aspect ratios were incorporated into a PAN-N,N-dimethylformamide system and the composite nanofibers reinforced with aligned ZnO rods up to 50 wt% were successfully electrospun, and subsequently, carbonized. The morphology and the structural analysis of the resultant carbon nanofibers revealed that the rigid ZnO nanorods, present inside the nanofibers, possibly acted as scaffolds (temporary support structures) for

  10. Membranes of MnO Beading in Carbon Nanofibers as Flexible Anodes for High-Performance Lithium-Ion Batteries

    NASA Astrophysics Data System (ADS)

    Zhao, Xin; Du, Yuxuan; Jin, Lei; Yang, Yang; Wu, Shuilin; Li, Weihan; Yu, Yan; Zhu, Yanwu; Zhang, Qinghua

    2015-09-01

    Freestanding yet flexible membranes of MnO/carbon nanofibers are successfully fabricated through incorporating MnO2 nanowires into polymer solution by a facile electrospinning technique. During the stabilization and carbonization processes of the as-spun membranes, MnO2 nanowires are transformed to MnO nanoparticles coincided with a conversion of the polymer from an amorphous state to a graphitic structure of carbon nanofibers. The hybrids consist of isolated MnO nanoparticles beading in the porous carbon and demonstrate superior performance when being used as a binder-free anode for lithium-ion batteries. With an optimized amount of MnO (34.6 wt%), the anode exhibits a reversible capacity of as high as 987.3 mAh g-1 after 150 discharge/charge cycles at 0.1 A g-1, a good rate capability (406.1 mAh g-1 at 3  A g-1) and an excellent cycling performance (655 mAh g-1 over 280 cycles at 0.5 A g-1). Furthermore, the hybrid anode maintains a good electrochemical performance at bending state as a flexible electrode.

  11. Membranes of MnO Beading in Carbon Nanofibers as Flexible Anodes for High-Performance Lithium-Ion Batteries

    PubMed Central

    Zhao, Xin; Du, Yuxuan; Jin, Lei; Yang, Yang; Wu, Shuilin; Li, Weihan; Yu, Yan; Zhu, Yanwu; Zhang, Qinghua

    2015-01-01

    Freestanding yet flexible membranes of MnO/carbon nanofibers are successfully fabricated through incorporating MnO2 nanowires into polymer solution by a facile electrospinning technique. During the stabilization and carbonization processes of the as-spun membranes, MnO2 nanowires are transformed to MnO nanoparticles coincided with a conversion of the polymer from an amorphous state to a graphitic structure of carbon nanofibers. The hybrids consist of isolated MnO nanoparticles beading in the porous carbon and demonstrate superior performance when being used as a binder-free anode for lithium-ion batteries. With an optimized amount of MnO (34.6 wt%), the anode exhibits a reversible capacity of as high as 987.3 mAh g−1 after 150 discharge/charge cycles at 0.1 A g−1, a good rate capability (406.1 mAh g−1 at 3  A g−1) and an excellent cycling performance (655 mAh g−1 over 280 cycles at 0.5 A g−1). Furthermore, the hybrid anode maintains a good electrochemical performance at bending state as a flexible electrode. PMID:26374601

  12. First Introduction of NiSe2 to Anode Material for Sodium-Ion Batteries: A Hybrid of Graphene-Wrapped NiSe2/C Porous Nanofiber

    PubMed Central

    Cho, Jung Sang; Lee, Seung Yeon; Kang, Yun Chan

    2016-01-01

    The first-ever study of nickel selenide materials as efficient anode materials for Na-ion rechargeable batteries is conducted using the electrospinning process. NiSe2-reduced graphene oxide (rGO)-C composite nanofibers are successfully prepared via electrospinning and a subsequent selenization process. The electrospun nanofibers giving rise to these porous-structured composite nanofibers with optimum amount of amorphous C are obtained from the polystyrene to polyacrylonitrile ratio of 1/4. These composite nanofibers also consist of uniformly distributed single-crystalline NiSe2 nanocrystals that have a mean size of 27 nm. In contrast, the densely structured bare NiSe2 nanofibers formed via selenization of the pure NiO nanofibers consist of large crystallites. The initial discharge capacities of the NiSe2-rGO-C composite and bare NiSe2 nanofibers at a current density of 200 mA g−1 are 717 and 755 mA h g−1, respectively. However, the respective 100th-cycle discharge capacities of the former and latter are 468 and 35 mA h g−1. Electrochemical impedance spectroscopy measurements reveal the structural stability of the composite nanofibers during repeated Na-ion insertion and extraction processes. The excellent Na-ion storage properties of these nanofibers are attributed to this structural stability. PMID:26997350

  13. First Introduction of NiSe2 to Anode Material for Sodium-Ion Batteries: A Hybrid of Graphene-Wrapped NiSe2/C Porous Nanofiber

    NASA Astrophysics Data System (ADS)

    Cho, Jung Sang; Lee, Seung Yeon; Kang, Yun Chan

    2016-03-01

    The first-ever study of nickel selenide materials as efficient anode materials for Na-ion rechargeable batteries is conducted using the electrospinning process. NiSe2-reduced graphene oxide (rGO)-C composite nanofibers are successfully prepared via electrospinning and a subsequent selenization process. The electrospun nanofibers giving rise to these porous-structured composite nanofibers with optimum amount of amorphous C are obtained from the polystyrene to polyacrylonitrile ratio of 1/4. These composite nanofibers also consist of uniformly distributed single-crystalline NiSe2 nanocrystals that have a mean size of 27 nm. In contrast, the densely structured bare NiSe2 nanofibers formed via selenization of the pure NiO nanofibers consist of large crystallites. The initial discharge capacities of the NiSe2-rGO-C composite and bare NiSe2 nanofibers at a current density of 200 mA g‑1 are 717 and 755 mA h g‑1, respectively. However, the respective 100th-cycle discharge capacities of the former and latter are 468 and 35 mA h g‑1. Electrochemical impedance spectroscopy measurements reveal the structural stability of the composite nanofibers during repeated Na-ion insertion and extraction processes. The excellent Na-ion storage properties of these nanofibers are attributed to this structural stability.

  14. First Introduction of NiSe2 to Anode Material for Sodium-Ion Batteries: A Hybrid of Graphene-Wrapped NiSe2/C Porous Nanofiber.

    PubMed

    Cho, Jung Sang; Lee, Seung Yeon; Kang, Yun Chan

    2016-01-01

    The first-ever study of nickel selenide materials as efficient anode materials for Na-ion rechargeable batteries is conducted using the electrospinning process. NiSe2-reduced graphene oxide (rGO)-C composite nanofibers are successfully prepared via electrospinning and a subsequent selenization process. The electrospun nanofibers giving rise to these porous-structured composite nanofibers with optimum amount of amorphous C are obtained from the polystyrene to polyacrylonitrile ratio of 1/4. These composite nanofibers also consist of uniformly distributed single-crystalline NiSe2 nanocrystals that have a mean size of 27 nm. In contrast, the densely structured bare NiSe2 nanofibers formed via selenization of the pure NiO nanofibers consist of large crystallites. The initial discharge capacities of the NiSe2-rGO-C composite and bare NiSe2 nanofibers at a current density of 200 mA g(-1) are 717 and 755 mA h g(-1), respectively. However, the respective 100(th)-cycle discharge capacities of the former and latter are 468 and 35 mA h g(-1). Electrochemical impedance spectroscopy measurements reveal the structural stability of the composite nanofibers during repeated Na-ion insertion and extraction processes. The excellent Na-ion storage properties of these nanofibers are attributed to this structural stability. PMID:26997350

  15. Processing, characterization and modeling of carbon nanofiber modified carbon/carbon composites

    NASA Astrophysics Data System (ADS)

    Samalot Rivera, Francis J.

    Carbon/Carbon (C/C) composites are used in high temperature applications because they exhibit excellent thermomechanical properties. There are several challenges associated with the processing of C/C composites that include long cycle times, formation of closed porosity within fabric woven architecture and carbonization induced cracks that can lead to reduction of mechanical properties. This work addresses various innovative approaches to reduce processing uncertainties and thereby improve thermomechanical properties of C/C by using vapor grown carbon nanofibers (VGCNFs) in conjunction with carbon fabric and precursor phenolic matrix. The different aspects of the proposed research contribute to understanding of the translation of VGCNFs properties in a C/C composite. The specific objectives of the research are; (a) To understand the mechanical properties and microstructural features of phenolic resin precursor with and without modification with VGCNFs; (b) To develop innovative processing concepts that incorporate VGCNFs by spraying them on carbon fabric and/or adding VGCNFs to the phenolic resin precursor; and characterizing the process induced thermal and mechanical properties; and (c) To develop a finite element model to evaluate the thermal stresses developed in the carbonization of carbon/phenolic with and without VGCNFs. Addition of VGCNFs to phenolic resin enhanced the thermal and physical properties in terms of flexure and interlaminar properties, storage modulus and glass transition temperature and lowered the coefficient of thermal expansion. The approaches of spraying VGCNFs on the fabric surface and mixing VGCNFs with the phenolic resin was found to be effective in enhancing mechanical and thermal properties of the resulting C/C composites. Fiber bridging, improved carbon yield and minimization of carbonization-induced damage were the benefits of incorporating VGCNFs in C/C composites. Carbonization induced matrix cracking predicted by the finite

  16. Method for production of carbon nanofiber mat or carbon paper

    SciTech Connect

    Naskar, Amit K.

    2015-08-04

    Method for the preparation of a non-woven mat or paper made of carbon fibers, the method comprising carbonizing a non-woven mat or paper preform (precursor) comprised of a plurality of bonded sulfonated polyolefin fibers to produce said non-woven mat or paper made of carbon fibers. The preforms and resulting non-woven mat or paper made of carbon fiber, as well as articles and devices containing them, and methods for their use, are also described.

  17. Cobalt/copper-decorated carbon nanofibers as novel non-precious electrocatalyst for methanol electrooxidation

    NASA Astrophysics Data System (ADS)

    Barakat, Nasser A. M.; El-Newehy, Mohamed; Al-Deyab, Salem S.; Kim, Hak Yong

    2014-01-01

    In this study, Co/Cu-decorated carbon nanofibers are introduced as novel electrocatalyst for methanol oxidation. The introduced nanofibers have been prepared based on graphitization of poly(vinyl alcohol) which has high carbon content compared to many polymer precursors for carbon nanofiber synthesis. Typically, calcination in argon atmosphere of electrospun nanofibers composed of cobalt acetate tetrahydrate, copper acetate monohydrate, and poly(vinyl alcohol) leads to form carbon nanofibers decorated by CoCu nanoparticles. The graphitization of the poly(vinyl alcohol) has been enhanced due to presence of cobalt which acts as effective catalyst. The physicochemical characterization affirmed that the metallic nanoparticles are sheathed by thin crystalline graphite layer. Investigation of the electrocatalytic activity of the introduced nanofibers toward methanol oxidation indicates good performance, as the corresponding onset potential was small compared to many reported materials; 310 mV (vs. Ag/AgCl electrode) and a current density of 12 mA/cm2 was obtained. Moreover, due to the graphite shield, good stability was observed. Overall, the introduced study opens new avenue for cheap and stable transition metals-based nanostructures as non-precious catalysts for fuel cell applications.

  18. Cobalt/copper-decorated carbon nanofibers as novel non-precious electrocatalyst for methanol electrooxidation

    PubMed Central

    2014-01-01

    In this study, Co/Cu-decorated carbon nanofibers are introduced as novel electrocatalyst for methanol oxidation. The introduced nanofibers have been prepared based on graphitization of poly(vinyl alcohol) which has high carbon content compared to many polymer precursors for carbon nanofiber synthesis. Typically, calcination in argon atmosphere of electrospun nanofibers composed of cobalt acetate tetrahydrate, copper acetate monohydrate, and poly(vinyl alcohol) leads to form carbon nanofibers decorated by CoCu nanoparticles. The graphitization of the poly(vinyl alcohol) has been enhanced due to presence of cobalt which acts as effective catalyst. The physicochemical characterization affirmed that the metallic nanoparticles are sheathed by thin crystalline graphite layer. Investigation of the electrocatalytic activity of the introduced nanofibers toward methanol oxidation indicates good performance, as the corresponding onset potential was small compared to many reported materials; 310 mV (vs. Ag/AgCl electrode) and a current density of 12 mA/cm2 was obtained. Moreover, due to the graphite shield, good stability was observed. Overall, the introduced study opens new avenue for cheap and stable transition metals-based nanostructures as non-precious catalysts for fuel cell applications. PMID:24387682

  19. Fabricating solid carbon porous electrodes from powders

    DOEpatents

    Kaschmitter, James L.; Tran, Tri D.; Feikert, John H.; Mayer, Steven T.

    1997-01-01

    Fabrication of conductive solid porous carbon electrodes for use in batteries, double layer capacitors, fuel cells, capacitive dionization, and waste treatment. Electrodes fabricated from low surface area (<50 m.sup.2 /gm) graphite and cokes exhibit excellent reversible lithium intercalation characteristics, making them ideal for use as anodes in high voltage lithium insertion (lithium-ion) batteries. Electrodes having a higher surface area, fabricated from powdered carbon blacks, such as carbon aerogel powder, carbon aerogel microspheres, activated carbons, etc. yield high conductivity carbon compositives with excellent double layer capacity, and can be used in double layer capacitors, or for capacitive deionization and/or waste treatment of liquid streams. By adding metallic catalysts to be high surface area carbons, fuel cell electrodes can be produced.

  20. Fabricating solid carbon porous electrodes from powders

    DOEpatents

    Kaschmitter, J.L.; Tran, T.D.; Feikert, J.H.; Mayer, S.T.

    1997-06-10

    Fabrication is described for conductive solid porous carbon electrodes for use in batteries, double layer capacitors, fuel cells, capacitive deionization, and waste treatment. Electrodes fabricated from low surface area (<50 m{sup 2}/gm) graphite and cokes exhibit excellent reversible lithium intercalation characteristics, making them ideal for use as anodes in high voltage lithium insertion (lithium-ion) batteries. Electrodes having a higher surface area, fabricated from powdered carbon blacks, such as carbon aerogel powder, carbon aerogel microspheres, activated carbons, etc. yield high conductivity carbon composites with excellent double layer capacity, and can be used in double layer capacitors, or for capacitive deionization and/or waste treatment of liquid streams. By adding metallic catalysts to high surface area carbons, fuel cell electrodes can be produced. 1 fig.

  1. Molecular monolayers for attaching electroactive molecules to vertically aligned carbon nanofibers

    NASA Astrophysics Data System (ADS)

    Landis, Elizabeth C.

    Integrating molecular monolayers with nanoscale carbon materials is attractive for a variety of applications including electroanalysis, sensing, and electrocatalysis due to the high stability and high surface area of nanoscale carbon. Vertically aligned carbon nanofibers are particularly interesting because their molecular structure indicates that they may have relatively reactive surfaces compared to other types of nanoscale carbon. This work explores the use of vertically aligned carbon nanofibers as a platform for electrocatalysis. We determined the morphology and binding locations of molecular layers on the nanofiber surface, then describe two methods for covalently binding electroactive molecules to the surface. The electron transfer process through the molecular layers was studied with emphasis on understanding the effects of the molecular linkage between the electroactive molecule and the surface and understanding the role of solvent and electrolyte in the electron transfer process. We determined that the electron transfer mechanism through monolayers on vertically aligned carbon nanofibers is controlled by the morphology of the molecular layers on the surface. Several potential catalysts were attached to the surface to evaluate the carbon nanofibers as scaffolds for electrocatalytic reactions.

  2. Hollow carbon nanofiber-encapsulated sulfur cathodes for high specific capacity rechargeable lithium batteries.

    PubMed

    Zheng, Guangyuan; Yang, Yuan; Cha, Judy J; Hong, Seung Sae; Cui, Yi

    2011-10-12

    Sulfur has a high specific capacity of 1673 mAh/g as lithium battery cathodes, but its rapid capacity fading due to polysulfides dissolution presents a significant challenge for practical applications. Here we report a hollow carbon nanofiber-encapsulated sulfur cathode for effective trapping of polysulfides and demonstrate experimentally high specific capacity and excellent electrochemical cycling of the cells. The hollow carbon nanofiber arrays were fabricated using anodic aluminum oxide (AAO) templates, through thermal carbonization of polystyrene. The AAO template also facilitates sulfur infusion into the hollow fibers and prevents sulfur from coating onto the exterior carbon wall. The high aspect ratio of the carbon nanofibers provides an ideal structure for trapping polysulfides, and the thin carbon wall allows rapid transport of lithium ions. The small dimension of these nanofibers provides a large surface area per unit mass for Li(2)S deposition during cycling and reduces pulverization of electrode materials due to volumetric expansion. A high specific capacity of about 730 mAh/g was observed at C/5 rate after 150 cycles of charge/discharge. The introduction of LiNO(3) additive to the electrolyte was shown to improve the Coulombic efficiency to over 99% at C/5. The results show that the hollow carbon nanofiber-encapsulated sulfur structure could be a promising cathode design for rechargeable Li/S batteries with high specific energy. PMID:21916442

  3. Preparation and characterization of carbon nanofiber-polymide composites

    NASA Astrophysics Data System (ADS)

    Li, Xiaobing

    Carbon nanofibers (CNFs) are potentially excellent reinforcements in polymer-based composites due to very good mechanical properties, thermal and electrical conductivity, and low cost to manufacture. The dispersion of fibers and the interfacial interaction with the polymer matrix need to be improved for CNF composites to achieve this potential. Treatment of the nanofiber surface with groups that are compatible with the polymer is key to addressing these issues. Attached functional groups may enhance the adhesion between reinforcement phase and matrix phase and reduce the slip of polymer chains on the surfaces of fibers. As a result, load can be transferred to fibers efficiently. In this investigation, CNFs were used as reinforcements in a polyimide (PI) matrix to produce a composite. To improve dispersion of fibers as well as interfacial adhesion, oxidized carbon nanofibers (OCNFs) were functionalized by covalently attaching 1,4-phenylenediamine (1,4-PDA) or polyimide oligomer to the surfaces. The functionalization with diamine was carried out either through direct reaction with OCNFs in dimethylacetimide (DMAc) solvent or through a two-step approach in which oxidized fibers were reacted with thionyl chloride (SOCl2) to improve surface reactivity followed by reaction with PDA in DMAc. The PDA was successfully bonded to the surfaces of fibers using both strategies. The further attachment of oligomer proceeded as expected in DMAc. The functionalized CNFs were characterized using Raman spectroscopy, thermal gravimetric analysis (TGA) and X-ray photoelectron spectroscopy (XPS) to confirm the functionalization reaction. Raman spectra and XPS spectra qualitatively indicated target chemical bonds were formed in each reaction step. Quantifications of TGA and XPS consistently supported that desired chemical moieties were present on the surfaces of fibers. In short, the interfaces of fibers were tailored with groups that would mimic the structure of polyimide and can

  4. Direct synthesis of mesostructured carbon nanofibers decorated with silver-nanoparticles as a multifunctional membrane for water treatment

    NASA Astrophysics Data System (ADS)

    Aboueloyoun Taha, Ahmed

    2015-12-01

    One-dimensional (1D) porous carbon nanofibers (CNFs) decorated by silver (Ag) nanoparticles (NPs) were prepared using a one-pot/self-template synthesis strategy by combining electrospinning and carbonization methods. The characterization results revealed that AgNPs were homogenously distributed along the CNFs and possessed a relatively uniform nano-size of about 12 nm. The novel membrane distinctively displayed enhanced photocatalytic activity under visible-light irradiation. The membrane exhibited excellent dye degradation and bacteria disinfection in batch experiments. The high photocatalytic activity can be attributed to the highly accessible surface areas, good light absorption capability, and high separation efficiency of photogenerated electron-hole pairs. The as-prepared membranes can be easily recycled because of their 1D property.

  5. Experimental study and modeling of swelling and bubble growth in carbon nanofiber filled mesophase pitch during carbonization

    NASA Astrophysics Data System (ADS)

    Calebrese, Christopher

    Graphite and all carbon bipolar plates show corrosion resistance in fuel cells and provide good electrical conductivity. These materials typically need to be individually machined, a time consuming and costly process. Mesophase pitch is used to manufacture carbon fibers and carbon-carbon composites. This material provides a good starting point for the production of a moldable, all carbon bipolar plate. However, processing of mesophase pitch to produce all carbon materials requires a time intensive oxidation step to prevent swelling during carbonization. In this work, carbon nanofibers were used to reduce swelling in mesophase pitch. It was found that the increase in viscosity with the addition of carbon nanofibers was responsible for the reduction in swelling. The influence of the filler became apparent above the percolation threshold. At loadings below the percolation threshold, the swelling of the mesophase pitch was not reduced after carbonization. The swelling of the mesophase pitch at a given carbon nanofiber loading was also dependent on the length of the carbon nanofibers. Longer carbon nanofibers led to greater increases in the viscosity of the melt and thus led to greater reduction in swelling. The final carbon product was evaluated for use as a low temperature fuel cell bipolar plate material. Constraining the mesophase pitch during carbonization led to a final product with strength and electrical conductivity comparable to current composite bipolar plate materials. The addition of micron size chopped glass fibers with a softening point near 850°C and carbon nanofibers led to a final product with air permeability less than that of graphite. A spherically symmetric, single bubble growth model was also developed. The model included temperature dependence, liquid to bubble mass transfer and reactions in the system. Results from simulations showed that that the increase in viscosity due to the addition of carbon nanofibers slows the growth of bubbles, but

  6. Pt/Carbon Nanofiber Nanocomposites as Electrocatalysts for Direct Methanol Fuel Cells: Prominent Effects of Carbon Nanofiber Nanostructures

    SciTech Connect

    Li, Zhizhou; Cui, Xiaoli; Zhang, Xinsheng; Wang, Qingfei; Shao, Yuyan; Lin, Yuehe

    2009-04-01

    Carbon nanofibers (CNFs) with different microstructures, including platelet-CNFs (PCNFs), fish-bone-CNFs, and tube-CNFs, were synthesized, characterized and evaluated toward methanol oxidation reaction (MOR). The CNFs studied here showed several structures in which various stacked morphologies as well as the ordering of their size and graphite layers can be well controlled. Platinum nanoparticles have been electrodeposited on CNFs surfaces, and their electrocatalytic activities toward MOR have been studied by using cyclic voltammetry, chronoamperometry, and linear sweep voltammograms. Morphologies, textural properties, and the crystalline structure of the CNFs supports and catalysts have been characterized with transmission electron microscopy and scanning electron microscopy. The comparative tests conclude that Pt/PCNFs have the best electrocatalytic performance and good stability at room temperature. The high electrocatalytic activity and stability can be attributed to the specific microstructure of PCNFs, which have large numbers of edge-active carbon atoms on the surface of the CNFs as well as synergistic effects between CNFs and the platinum nanoparticles. The results suggest that PCNFs are excellent potential candidates as catalyst supports in direct methanol fuel cells.

  7. Application of packed porous nanofibers-solid-phase extraction for the detection of sulfonamide residues from environmental water samples by ultra high performance liquid chromatography with mass spectrometry.

    PubMed

    Chen, Rong; Yang, Yingying; Wang, Na; Hao, Lijun; Li, Li; Guo, Xinyan; Zhang, Junchi; Hu, Yuzhu; Shen, Weiyang

    2015-03-01

    Porous electrospun nanofibers, as new materials for solid-phase extraction, were synthesized by electrospinning and coupled with ultra high performance liquid chromatography and mass spectrometry to determine sulfonamide residues in environmental water. Aligned porous polystyrene electrospun nanofibers were fabricated under the mechanism of phase separation. The high-specific surface of these nanofibers (70 m(2)/g) could improve recoveries of the target sulfonamides 4-10 times compared with that of polystyrene nonporous material (3.8 m(2)/g). Under the optimized conditions, 13 sulfonamide residues showed an excellent linear relationship in the range of 0.125-12.5 ng/mL with a linear correlation coefficient (r(2)) greater than 0.99, and the detection limits of sulfonamides were as low as 0.80-5.0 ng/L. Compared to the commercial C18 and HLB columns, the homemade porous nanofibers columns had some merits including simple fabrication and extraction process, short process time and environmental friendliness. The optimized method was applied to eight water samples collected from different livestock farms (Xuzhou, China). The results showed that polystyrene porous nanofibers were promising to preconcentrate sulfonamides of different polarities in the waste water. PMID:25546059

  8. Graphitic Carbon Nitride/Nitrogen-Rich Carbon Nanofibers: Highly Efficient Photocatalytic Hydrogen Evolution without Cocatalysts.

    PubMed

    Han, Qing; Wang, Bing; Gao, Jian; Qu, Liangti

    2016-08-26

    An interconnected framework of mesoporous graphitic-C3 N4 nanofibers merged with in situ incorporated nitrogen-rich carbon has been prepared. The unique composition and structure of the nanofibers as well as strong coupling between the components endow them with efficient light-harvesting properties, improved charged separation, and a multidimensional electron transport path that enhance the performance of hydrogen production. The as-obtained catalyst exhibits an extremely high hydrogen-evolution rate of 16885 μmol h(-1)  g(-1) , and a remarkable apparent quantum efficiency of 14.3 % at 420 nm without any cocatalysts, which is much higher than most reported g-C3 N4 -based photocatalysts even in the presence of Pt-based cocatalysts. PMID:27467255

  9. CMOS compatible on-chip decoupling capacitor based on vertically aligned carbon nanofibers

    NASA Astrophysics Data System (ADS)

    Saleem, A. M.; Göransson, G.; Desmaris, V.; Enoksson, P.

    2015-05-01

    On-chip decoupling capacitor of specific capacitance 55 pF/μm2 (footprint area) which is 10 times higher than the commercially available discrete and on-chip (65 nm technology node) decoupling capacitors is presented. The electrodes of the capacitor are based on vertically aligned carbon nanofibers (CNFs) capable of being integrated directly on CMOS chips. The carbon nanofibers employed in this study were grown on CMOS chips using direct current plasma enhanced chemical vapor deposition (DC-PECVD) technique at CMOS compatible temperature. The carbon nanofibers were grown at temperature from 390 °C to 550 °C. The capacitance of the carbon nanofibers was measured by cyclic voltammetry and thus compared. Futhermore the capacitance of decoupling capacitor was measured using different voltage scan rate to show their high charge storage capability and finally the cyclic voltammetry is run for 1000 cycles to assess their suitability as electrode material for decoupling capacitor. Our results show the high specific capacitance and long-term reliability of performance of the on-chip decoupling capacitors. Moreover, the specific capacitance shown is larger for carbon nanofibers grown at higher temperature.

  10. A novel nano-nonwoven fabric with three-dimensionally dispersed nanofibers: entrapment of carbon nanofibers within nonwovens using the wet-lay process

    NASA Astrophysics Data System (ADS)

    Karwa, Amogh N.; Barron, Troy J.; Davis, Virginia A.; Tatarchuk, Bruce J.

    2012-05-01

    This study demonstrates, for the first time, the manufacturing of novel nano-nonwovens that are comprised of three-dimensionally distributed carbon nanofibers within the matrices of traditional wet-laid nonwovens. The preparation of these nano-nonwovens involves dispersing and flocking carbon nanofibers, and optimizing colloidal chemistry during wet-lay formation. The distribution of nanofibers within the nano-nonwoven was verified using polydispersed aerosol filtration testing, air permeability, low surface tension liquid capillary porometry, SEM and cyclic voltammetry. All these characterization techniques indicated that nanofiber flocks did not behave as large solid clumps, but retained the ‘nanoporous’ structure expected from nanofibers. These nano-nonwovens showed significant enhancements in aerosol filtration performance. The reduction-oxidation reactions of the functional groups on nanofibers and the linear variation of electric double-layer capacitance with nanofiber loading were measured using cyclic voltammetry. More than 65 m2 (700 ft2) of the composite were made during the demonstration of process scalability using a Fourdrinier-type continuous pilot papermaking machine. The scalability of the process with the control over pore size distribution makes these composites very promising for filtration and other nonwoven applications.

  11. A novel nano-nonwoven fabric with three-dimensionally dispersed nanofibers: entrapment of carbon nanofibers within nonwovens using the wet-lay process.

    PubMed

    Karwa, Amogh N; Barron, Troy J; Davis, Virginia A; Tatarchuk, Bruce J

    2012-05-11

    This study demonstrates, for the first time, the manufacturing of novel nano-nonwovens that are comprised of three-dimensionally distributed carbon nanofibers within the matrices of traditional wet-laid nonwovens. The preparation of these nano-nonwovens involves dispersing and flocking carbon nanofibers, and optimizing colloidal chemistry during wet-lay formation. The distribution of nanofibers within the nano-nonwoven was verified using polydispersed aerosol filtration testing, air permeability, low surface tension liquid capillary porometry, SEM and cyclic voltammetry. All these characterization techniques indicated that nanofiber flocks did not behave as large solid clumps, but retained the 'nanoporous' structure expected from nanofibers. These nano-nonwovens showed significant enhancements in aerosol filtration performance. The reduction-oxidation reactions of the functional groups on nanofibers and the linear variation of electric double-layer capacitance with nanofiber loading were measured using cyclic voltammetry. More than 65 m² (700 ft²) of the composite were made during the demonstration of process scalability using a Fourdrinier-type continuous pilot papermaking machine. The scalability of the process with the control over pore size distribution makes these composites very promising for filtration and other nonwoven applications. PMID:22498976

  12. Effects of carbon nanofiber on physiology of Drosophila

    PubMed Central

    Lee, Shin-Hae; Lee, Hye-Yeon; Lee, Eun-Ji; Khang, Dongwoo; Min, Kyung-Jin

    2015-01-01

    As nanomaterials are now widely utilized in a wide range of fields for both medical and industrial applications, concerns over their potential toxicity to human health and the environment have increased. To evaluate the toxicity of long-term exposure to carbon nanofibers (CNFs) in an in vivo system, we selected Drosophila melanogaster as a model organism. Oral administration of CNFs at a concentration of 1,000 μg/mL had adverse effects on fly physiology. Long-term administration of a high dose of CNFs (1,000 μg/mL) reduced larval viability based on the pupa:egg ratio, adult fly lifespan, reproductive activity, climbing activity, and survival rate in response to starvation stress. However, CNFs at a low concentration (100 μg/mL) did not show any significant deleterious effect on developmental rate or fecundity. Furthermore, long-term administration of a low dose of CNFs (100 μg/mL) increased lifespan and climbing ability, coincident with mild reactive oxygen species generation and stimulation of the antioxidant system. Taken together, our data suggest that a high dose of CNFs has obvious physiological toxicity, whereas low-dose chronic exposure to CNFs can actually have beneficial effects via stimulation of the antioxidant defense system. PMID:26056448

  13. Manipulation of Bacteriophages with Dielectrophoresis on Carbon Nanofiber Nanoelectrode Arrays

    PubMed Central

    Madiyar, Foram Ranjeet; Syed, Lateef Uddin; Culbertson, Christopher; Li, Jun

    2013-01-01

    This work describes efficient manipulation of bacteriophage virus particles using a nanostructured dielectrophoresis (DEP) device. The non-uniform electric field for DEP is created by utilizing a nanoelectrode array (NEA) made of vertically aligned carbon nanofibers (VACNFs) versus a macroscopic indium tin oxide electrode in a “points-and-lid” configuration integrated in a microfluidic channel. The capture of the virus particles has been systematically investigated versus the flow velocity, sinusoidal AC frequency, peak-to-peak voltage, and virus concentration. The DEP capture at all conditions is reversible and the captured virus particles are released immediately when the voltage is turned off. At the low virus concentration (8.9×104 pfu·ml−1), the DEP capture efficiency up to 60% can be obtained. The virus particles are individually captured at isolated nanoelectrode tips and accumulate linearly with time. Due to the comparable size, it is more effective to capture virus particles than larger bacterial cells with such NEA based DEP devices. This technique can be potentially utilized as a fast sample preparation module in a microfluidic chip to capture, separate, and concentrate viruses and other biological particles in small volumes of dilute solutions in a portable detection system for field applications. PMID:23348683

  14. Effect of twist and porosity on the electrical conductivity of carbon nanofiber yarns

    NASA Astrophysics Data System (ADS)

    Chawla, S.; Naraghi, M.; Davoudi, A.

    2013-06-01

    This study focuses on the effect of twist and porosity on the electrical conductivity of carbon nanofiber (CNF) yarns. The process of fabrication of CNF yarns included the synthesis of aligned ribbons of polyacrylonitrile (PAN) nanofibers via electrospinning. The PAN ribbons were twisted into yarns with twist levels ranging from zero twist to high twists of 1300 turn per meter (tpm). The twist imposed on the ribbons substantially improved the interactions between nanofibers and reduced the porosity. The PAN yarns were subsequently stabilized in air, and then carbonized in nitrogen at 1100 ° C for 1 h. Compressive stresses developed between the PAN nanofibers as a result of twist promoted interfusion between neighboring nanofibers, which was accelerated by heating the yarns during stabilization to temperatures above the glass transition of PAN. The electrical conductivity of the yarns was measured with a four point probe measurement technique. Although increasing the twist promotes electrical conductivity between nanofibers by forming junctions between them, our results indicate that the electrical conductivity does not continuously increase with increasing twist, but reaches a threshold value after which it starts to decrease. The causes for this behavior were studied through experimental techniques and further explored using a yarn-equivalent electrical circuit model.

  15. Towards Scalable Binderless Electrodes: Carbon Coated Silicon Nanofiber Paper via Mg Reduction of Electrospun SiO2 Nanofibers

    PubMed Central

    Favors, Zachary; Bay, Hamed Hosseini; Mutlu, Zafer; Ahmed, Kazi; Ionescu, Robert; Ye, Rachel; Ozkan, Mihrimah; Ozkan, Cengiz S.

    2015-01-01

    The need for more energy dense and scalable Li-ion battery electrodes has become increasingly pressing with the ushering in of more powerful portable electronics and electric vehicles (EVs) requiring substantially longer range capabilities. Herein, we report on the first synthesis of nano-silicon paper electrodes synthesized via magnesiothermic reduction of electrospun SiO2 nanofiber paper produced by an in situ acid catalyzed polymerization of tetraethyl orthosilicate (TEOS) in-flight. Free-standing carbon-coated Si nanofiber binderless electrodes produce a capacity of 802 mAh g−1 after 659 cycles with a Coulombic efficiency of 99.9%, which outperforms conventionally used slurry-prepared graphite anodes by over two times on an active material basis. Silicon nanofiber paper anodes offer a completely binder-free and Cu current collector-free approach to electrode fabrication with a silicon weight percent in excess of 80%. The absence of conductive powder additives, metallic current collectors, and polymer binders in addition to the high weight percent silicon all contribute to significantly increasing capacity at the cell level. PMID:25655007

  16. Towards scalable binderless electrodes: carbon coated silicon nanofiber paper via Mg reduction of electrospun SiO2 nanofibers.

    PubMed

    Favors, Zachary; Bay, Hamed Hosseini; Mutlu, Zafer; Ahmed, Kazi; Ionescu, Robert; Ye, Rachel; Ozkan, Mihrimah; Ozkan, Cengiz S

    2015-01-01

    The need for more energy dense and scalable Li-ion battery electrodes has become increasingly pressing with the ushering in of more powerful portable electronics and electric vehicles (EVs) requiring substantially longer range capabilities. Herein, we report on the first synthesis of nano-silicon paper electrodes synthesized via magnesiothermic reduction of electrospun SiO2 nanofiber paper produced by an in situ acid catalyzed polymerization of tetraethyl orthosilicate (TEOS) in-flight. Free-standing carbon-coated Si nanofiber binderless electrodes produce a capacity of 802 mAh g(-1) after 659 cycles with a Coulombic efficiency of 99.9%, which outperforms conventionally used slurry-prepared graphite anodes by over two times on an active material basis. Silicon nanofiber paper anodes offer a completely binder-free and Cu current collector-free approach to electrode fabrication with a silicon weight percent in excess of 80%. The absence of conductive powder additives, metallic current collectors, and polymer binders in addition to the high weight percent silicon all contribute to significantly increasing capacity at the cell level. PMID:25655007

  17. Towards Scalable Binderless Electrodes: Carbon Coated Silicon Nanofiber Paper via Mg Reduction of Electrospun SiO2 Nanofibers

    NASA Astrophysics Data System (ADS)

    Favors, Zachary; Bay, Hamed Hosseini; Mutlu, Zafer; Ahmed, Kazi; Ionescu, Robert; Ye, Rachel; Ozkan, Mihrimah; Ozkan, Cengiz S.

    2015-02-01

    The need for more energy dense and scalable Li-ion battery electrodes has become increasingly pressing with the ushering in of more powerful portable electronics and electric vehicles (EVs) requiring substantially longer range capabilities. Herein, we report on the first synthesis of nano-silicon paper electrodes synthesized via magnesiothermic reduction of electrospun SiO2 nanofiber paper produced by an in situ acid catalyzed polymerization of tetraethyl orthosilicate (TEOS) in-flight. Free-standing carbon-coated Si nanofiber binderless electrodes produce a capacity of 802 mAh g-1 after 659 cycles with a Coulombic efficiency of 99.9%, which outperforms conventionally used slurry-prepared graphite anodes by over two times on an active material basis. Silicon nanofiber paper anodes offer a completely binder-free and Cu current collector-free approach to electrode fabrication with a silicon weight percent in excess of 80%. The absence of conductive powder additives, metallic current collectors, and polymer binders in addition to the high weight percent silicon all contribute to significantly increasing capacity at the cell level.

  18. Facile electrospinning preparation of phosphorus and nitrogen dual-doped cobalt-based carbon nanofibers as bifunctional electrocatalyst

    NASA Astrophysics Data System (ADS)

    Wang, Zhuang; Zuo, Pengjian; Fan, Liquan; Han, Jianan; Xiong, Yueping; Yin, Geping

    2016-04-01

    A novel electrochemical catalyst of phosphorus and nitrogen dual-doped cobalt-based carbon nanofibers (Cosbnd Nsbnd P-CNFs) is prepared by a facile and cost-effective electrospinning technique. Excellent features of the porous carbon nanofibers with large amounts of Co atoms, N/P-doping effect, abundant pyridinic-N and Cosbnd Nx clusters as catalytic active sites, and the advantages of the structure and composition result in a high catalytic efficiency. In alkaline or acidic media, Cosbnd Nsbnd P-CNFs exhibits remarkable electrocatalytic activities and kinetics for oxygen reduction reaction (ORR), superior methanol tolerance and stability, and a similar four-electron pathway. In addition, Cosbnd Nsbnd P-CNFs also shows excellent performance for hydrogen evolution reaction (HER), offering a low onset potential of -0.216 V and a stable current density of 10 mA cm-2 at potential of -0.248 V. The mechanism of ORR and HER catalytic active site arises from the doping of N/P atoms in the Co-based CNFs, which is responsible for the excellent electrocatalytic performance. Due to the excellent catalytic efficiencies, Cosbnd Nsbnd P-CNFs act as a promising catalyst material for fuel cells and water splitting technologies.

  19. High-performance supercapacitor electrode from cellulose-derived, inter-bonded carbon nanofibers

    NASA Astrophysics Data System (ADS)

    Cai, Jie; Niu, Haitao; Wang, Hongxia; Shao, Hao; Fang, Jian; He, Jingren; Xiong, Hanguo; Ma, Chengjie; Lin, Tong

    2016-08-01

    Carbon nanofibers with inter-bonded fibrous structure show high supercapacitor performance when being used as electrode materials. Their preparation is highly desirable from cellulose through a pyrolysis technique, because cellulose is an abundant, low cost natural material and its carbonization does not emit toxic substance. However, interconnected carbon nanofibers prepared from electrospun cellulose nanofibers and their capacitive behaviors have not been reported in the research literature. Here we report a facile one-step strategy to prepare inter-bonded carbon nanofibers from partially hydrolyzed cellulose acetate nanofibers, for making high-performance supercapacitors as electrode materials. The inter-fiber connection shows considerable improvement in electrode electrochemical performances. The supercapacitor electrode has a specific capacitance of ∼241.4 F g-1 at 1 A g-1 current density. It maintains high cycling stability (negligible 0.1% capacitance reduction after 10,000 cycles) with a maximum power density of ∼84.1 kW kg-1. They may find applications in the development of efficient supercapacitor electrodes for energy storage applications.

  20. Carbon nanofiber-based luminol-biotin probe for sensitive chemiluminescence detection of protein.

    PubMed

    Baj, Stefan; Krawczyk, Tomasz; Pradel, Natalia; Azam, Md Golam; Shibata, Takayuki; Dragusha, Shpend; Skutil, Krzysztof; Pawlyta, Miroslawa; Kai, Masaaki

    2014-01-01

    A carbon nanofiber-based luminol-biotin probe was synthesized for the sensitive chemiluminescence (CL) detection of a target protein by grafting luminol and biotin onto an oxidized carbon nanofiber. This carbon nanofiber was prepared by chemical vapor-deposition with methane in the presence of the Ni-Cu-MgO catalyst, which was followed by oxidization with HNO3-H2SO4 to produce a carboxyl group on the surface of the nanofiber. The material was grafted with luminol and biotin by means of a standard carbodiimide activation of COOH groups to produce corresponding amides. The substance was water-soluble and thus could be utilized as a sensitive CL probe for a protein assay. The probe showed highly specific affinity towards the biotin-labeled antibody via a streptavidin-biotin interaction. The detection limit for this model assay was approximately 0.2 pmol of the biotinized IgG spotted on a polyvinylidene fluoride (PVDF) membrane. Nonspecific binding to other proteins was not observed. Therefore, the synthesized carbon nanofiber-based CL probe may be useful for a sensitive and specific analysis of the target protein. PMID:25382040

  1. Functionalization of carbon nanotube and nanofiber electrodes with biological macromolecules: Progress toward a nanoscale biosensor

    NASA Astrophysics Data System (ADS)

    Baker, Sarah E.

    The integration of nanoscale carbon-based electrodes with biological recognition and electrical detection promises unparalleled biological detection systems. First, biologically modified carbon-based materials have been shown to have superior long-term chemical stability when compared to other commonly used materials for biological detection such as silicon, gold, and glass surfaces. Functionalizing carbon electrodes for biological recognition and using electrochemical methods to transduce biological binding information will enable real-time, hand-held, lower cost and stable biosensing devices. Nanoscale carbon-based electrodes allow the additional capability of fabricating devices with high densities of sensing elements, enabling multi-analyte detection on a single chip. We have worked toward the integration of these sensor components by first focusing on developing and characterizing the chemistry required to functionalize single-walled carbon nanotubes and vertically aligned carbon nanofibers with oligonucleotides and proteins for specific biological recognition. Chemical, photochemical and electrochemical methods for functionalizing these materials with biological molecules were developed. We determined, using fluorescence and colorimetric techniques, that these biologically modified nanoscale carbon electrodes are biologically active, selective, and stable. A photochemical functionalization method enabled facile functionalization of dense arrays vertically aligned carbon nanofiber forests. We found that much of the vertically aligned carbon nanofiber sidewalls were functionalized and biologically accessible by this method---the absolute number of DNA molecules hybridized to DNA-functionalized nanofiber electrodes was ˜8 times higher than the number of DNA molecules hybridized to flat glassy carbon electrodes and implies that nanofiber forest sensors may facilitate higher sensitivity to target DNA sequences per unit area. We also used the photochemical method

  2. Carbon Nanotubes/Nanofibers by Plasma Enhanced Chemical Vapour Deposition

    NASA Technical Reports Server (NTRS)

    Teo, K. B. K.; Hash, D. B.; Bell, M. S.; Chhowalla, M.; Cruden, B. A.; Amaratunga, G. A. J.; Meyyappan, M.; Milne, W. I.

    2005-01-01

    Plasma enhanced chemical vapour deposition (PECVD) has been recently used for the production of vertically aligned carbon nanotubedfibers (CN) directly on substrates. These structures are potentially important technologically as electron field emitters (e.g. microguns, microwave amplifiers, displays), nanoelectrodes for sensors, filter media, superhydrophobic surfaces and thermal interface materials for microelectronics. A parametric study on the growth of CN grown by glow discharge dc-PECVD is presented. In this technique, a substrate containing thin film Ni catalyst is exposed to C2H2 and NH3 gases at 700 C. Without plasma, this process is essentially thermal CVD which produces curly spaghetti-like CN as seen in Fig. 1 (a). With the plasma generated by biasing the substrate at -6OOV, we observed that the CN align vertically during growth as shown in Fig. l(b), and that the magnitude of the applied substrate bias affects the degree of alignment. The thickness of the thin film Ni catalyst was found to determine the average diameter and inversely the length of the CN. The yield and density of the CN were controlled by the use of different diffusion barrier materials under the Ni catalyst. Patterned CN growth [Fig. l(c)], with la variation in CN diameter of 4.1% and 6.3% respectively, is achieved by lithographically defining the Ni thin film prior to growth. The shape of the structures could be varied from very straight nanotube-like to conical tip-like nanofibers by increasing the ratio of C2H2 in the gas flow. Due to the plasma decomposition of C2H2, amorphous carbon (a-C) is an undesirable byproduct which could coat the substrate during CN growth. Using a combination of depth profiled Auger electron spectroscopy to study the substrate and in-situ mass spectroscopy to examine gas phase neutrals and ions, the optimal conditions for a-C free growth of CN is determined.

  3. Extraordinary improvement of the graphitic structure of continuous carbon nanofibers templated with double wall carbon nanotubes.

    PubMed

    Papkov, Dimitry; Beese, Allison M; Goponenko, Alexander; Zou, Yan; Naraghi, Mohammad; Espinosa, Horacio D; Saha, Biswajit; Schatz, George C; Moravsky, Alexander; Loutfy, Raouf; Nguyen, Sonbinh T; Dzenis, Yuris

    2013-01-22

    Carbon nanotubes are being widely studied as a reinforcing element in high-performance composites and fibers at high volume fractions. However, problems with nanotube processing, alignment, and non-optimal stress transfer between the nanotubes and surrounding matrix have so far prevented full utilization of their superb mechanical properties in composites. Here, we present an alternative use of carbon nanotubes, at a very small concentration, as a templating agent for the formation of graphitic structure in fibers. Continuous carbon nanofibers (CNF) were manufactured by electrospinning from polyacrylonitrile (PAN) with 1.2% of double wall nanotubes (DWNT). Nanofibers were oxidized and carbonized at temperatures from 600 °C to 1850 °C. Structural analyses revealed significant improvements in graphitic structure and crystal orientation in the templated CNFs, with the largest improvements observed at lower carbonization temperatures. In situ pull-out experiments showed good interfacial bonding between the DWNT bundles and the surrounding templated carbon matrix. Molecular Dynamics (MD) simulations of templated carbonization confirmed oriented graphitic growth and provided insight into mechanisms of carbonization initiation. The obtained results indicate that global templating of the graphitic structure in fine CNFs can be achieved at very small concentrations of well-dispersed DWNTs. The outcomes reveal a simple and inexpensive route to manufacture continuous CNFs with improved structure and properties for a variety of mechanical and functional applications. The demonstrated improvement of graphitic order at low carbonization temperatures in the absence of stretch shows potential as a promising new manufacturing technology for next generation carbon fibers. PMID:23249440

  4. Effect of carbon nanofibers on the infiltration and thermal conductivity of carbon/carbon composites

    SciTech Connect

    Li, Jinsong; Luo, Ruiying; Yan, Ying

    2011-09-15

    Highlights: {yields} The CNFs improve the infiltration rate and thermal properties of carbon/carbon composites. {yields} The densification rate increases with the CNF content increasing at the beginning of infiltration. {yields} The values of the thermal conductivity of the composite obtain their maximum values at 5 wt.%. -- Abstract: Preforms containing 0, 5, 10, 15 and 20 wt.% carbon nanofibers (CNFs) were fabricated by spreading layers of carbon cloth, and infiltrated using the electrified preform heating chemical vapor infiltration method (ECVI) under atmospheric pressure. Initial thermal gradients were determined. Resistivity and density evolutions with infiltration time have been recorded. Scanning electron microscopy, polarized light micrograph and X-ray diffraction technique were used to analyze the experiment results. The results showed that the infiltration rate increased with the rising of CNF content, and after 120 h of infiltration, the density was the highest when the CNF content was 5 wt.%, but the composite could not be densified efficiently as the CNF content ranged from 10 wt.% to 20 wt.%. CNF-reinforced C/C composites have enhanced thermal conductivity, the values at 5 wt.% were increased by nearly 5.5-24.1% in the X-Y direction and 153.8-251.3% in the Z direction compared to those with no CNFs. When the additive content was increased to 20 wt.%, due to the holes and cavities in the CNF web and between carbon cloth and matrix, the thermal conductivities in the X-Y and Z directions decreased from their maximum values at 5 wt.%.

  5. High performance supercapacitor based on Ni3S2/carbon nanofibers and carbon nanofibers electrodes derived from bacterial cellulose

    NASA Astrophysics Data System (ADS)

    Yu, Wendan; Lin, Worong; Shao, Xiaofeng; Hu, Zhaoxia; Li, Ruchun; Yuan, Dingsheng

    2014-12-01

    The Ni3S2 nanoparticles have been successfully grown on the carbon nanofibers (CNFs) derived from bacterial cellulose via a hydrothermal method, which the as-prepared composite exhibited high specific capacitance (883 F g-1 at 2 A g-1), much more than CNFs (108 F g-1 at 2 A g-1), and good cycle stability. The asymmetric supercapacitor was designed to contain the CNFs coated Ni3S2 nanoparticles (Ni3S2/CNFs) as positive electrode and CNFs as negative electrode in 2 M KOH electrolyte. Due to the synergistic effects of the two electrodes, asymmetric cell showed superior electrochemical performances. The optimized asymmetric supercapacitor gave a operating potential of 1.7 V in 2 M KOH aqueous solution, exhibiting a high specific capacitance of 56.6 F g-1 at 1 A g-1 and considerably high energy density of 25.8 Wh kg-1 at a power density of 425 W kg-1. Meanwhile, Ni3S2/CNFs//CNFs asymmetric supercapacitor showed excellent cycling stability with 97% specific capacitance retained after 2500 cycles.

  6. Genotoxicity of carbon nanofibers: are they potentially more or less dangerous than carbon nanotubes or asbestos?

    PubMed Central

    Kisin, E. R.; Murray, A.R.; Sargent, L.; Lowry, D.; Chirila, M.; Siegrist, K.J.; Schwegler-Berry, D.; Leonard, S.; Castranova, V.; Fadeel, B.; Kagan, V.E.; Shvedova, A.A.

    2011-01-01

    The production of carbon nanofibers and nanotubes (CNF/CNT) and their composite products is increasing globally. CNF are generating great interest in industrial sectors such as energy production and electronics, where alternative materials may have limited performance or are produced at a much higher cost. However, despite the increasing industrial use of carbon nanofibers, information on their potential adverse health effects is limited. In the current study, we examine the cytotoxic and genotoxic potential of carbon-based nanofibers (Pyrograf®-III) and compare this material with the effects of asbestos fibers (crocidolite) or single-walled carbon nanotubes (SWCNT). The genotoxic effects in the lung fibroblast (V79) cell line were examined using two complementary assays: the comet assay and micronucleus (MN) test. In addition, we utilized fluorescence in situ hybridization to detect the chromatin pan-centromeric signals within the MN indicating their origin by aneugenic (chromosomal malsegregation) or clastogenic (chromosome breakage) mechanisms. Cytotoxicity tests revealed a concentration- and time-dependent loss of V79 cell viability after exposure to all tested materials in the following sequence: asbestos>CNF>SWCNT. Additionally, cellular uptake and generation of oxygen radicals was seen in the murine RAW264.7 macrophages following exposure to CNF or asbestos but not after administration of SWCNT. DNA damage and MN induction were found after exposure to all tested materials with the strongest effect seen for CNF. Finally, we demonstrated that CNF induced predominately centromere-positive MN in primary human small airway epithelial cells (SAEC) indicating aneugenic events. Further investigations are warranted to elucidate the possible mechanisms involved in CNF-induced genotoxicity. PMID:21310169

  7. Genotoxicity of carbon nanofibers: Are they potentially more or less dangerous than carbon nanotubes or asbestos?

    SciTech Connect

    Kisin, E.R.; Murray, A.R.; Sargent, L.; Lowry, D.; Chirila, M.; Siegrist, K.J.; Schwegler-Berry, D.; Leonard, S.; Castranova, V.; Fadeel, B.; Kagan, V.E.; Shvedova, A.A.

    2011-04-01

    The production of carbon nanofibers and nanotubes (CNF/CNT) and their composite products is increasing globally. CNF are generating great interest in industrial sectors such as energy production and electronics, where alternative materials may have limited performance or are produced at a much higher cost. However, despite the increasing industrial use of carbon nanofibers, information on their potential adverse health effects is limited. In the current study, we examine the cytotoxic and genotoxic potential of carbon-based nanofibers (Pyrograf (registered) -III) and compare this material with the effects of asbestos fibers (crocidolite) or single-walled carbon nanotubes (SWCNT). The genotoxic effects in the lung fibroblast (V79) cell line were examined using two complementary assays: the comet assay and micronucleus (MN) test. In addition, we utilized fluorescence in situ hybridization to detect the chromatin pan-centromeric signals within the MN indicating their origin by aneugenic (chromosomal malsegregation) or clastogenic (chromosome breakage) mechanisms. Cytotoxicity tests revealed a concentration- and time-dependent loss of V79 cell viability after exposure to all tested materials in the following sequence: asbestos > CNF > SWCNT. Additionally, cellular uptake and generation of oxygen radicals was seen in the murine RAW264.7 macrophages following exposure to CNF or asbestos but not after administration of SWCNT. DNA damage and MN induction were found after exposure to all tested materials with the strongest effect seen for CNF. Finally, we demonstrated that CNF induced predominately centromere-positive MN in primary human small airway epithelial cells (SAEC) indicating aneugenic events. Further investigations are warranted to elucidate the possible mechanisms involved in CNF-induced genotoxicity.

  8. Mesoporous Carbon Nanofibers Embedded with MoS2 Nanocrystals for Extraordinary Li-Ion Storage.

    PubMed

    Hu, Shan; Chen, Wen; Uchaker, Evan; Zhou, Jing; Cao, Guozhong

    2015-12-01

    MoS2 nanocrystals embedded in mesoporous carbon nanofibers are synthesized through an electrospinning process followed by calcination. The resultant nanofibers are 100-150 nm in diameter and constructed from MoS2 nanocrystals with a lateral diameter of around 7 nm with specific surface areas of 135.9 m(2)  g(-1) . The MoS2 @C nanofibers are treated at 450 °C in H2 and comparison samples annealed at 800 °C in N2 . The heat treatments are designed to achieve good crystallinity and desired mesoporous microstructure, resulting in enhanced electrochemical performance. The small amount of oxygen in the nanofibers annealed in H2 contributes to obtaining a lower internal resistance, and thus, improving the conductivity. The results show that the nanofibers obtained at 450 °C in H2 deliver an extraordinary capacity of 1022 mA h g(-1) and improved cyclic stability, with only 2.3 % capacity loss after 165 cycles at a current density of 100 mA g(-1) , as well as an outstanding rate capability. The greatly improved kinetics and cycling stability of the mesoporous MoS2 @C nanofibers can be attributed to the crosslinked conductive carbon nanofibers, the large specific surface area, the good crystallinity of MoS2 , and the robust mesoporous microstructure. The resulting nanofiber electrodes, with short mass- and charge-transport pathways, improved electrical conductivity, and large contact area exposed to electrolyte, permitting fast diffusional flux of Li ions, explains the improved kinetics of the interfacial charge-transfer reaction and the diffusivity of the MoS2 @C mesoporous nanofibers. It is believed that the integration of MoS2 nanocrystals and mesoporous carbon nanofibers may have a synergistic effect, giving a promising anode, and widening the applicability range into high performance and mass production in the Li-ion battery market. PMID:26515375

  9. Synthesis of vertically aligned carbon nanofibers for interfacing with live systems

    SciTech Connect

    Melechko, Anatoli Vasilievich; Desikan, Ramya; McKnight, Timothy E; Klein, Kate L; Rack, P. D.

    2009-01-01

    The ability to synthesize carbon nanofibers with a high degree of control over their geometry, location, and structure via catalytic plasma-enhanced chemical vapor deposition has expanded the possibility of new applications. The nanoscale dimensions and high aspect ratio of vertically aligned carbon nanofibers (VACNFs), along with favorable physical and chemical characteristics, has provided a nanostructured material with properties that are well-suited for interfacing with live cells and tissues. This review surveys the aspects of synthesis, integration, and functionalization of VACNFs, followed by examples of how VACNFs have been used to interface with live systems for a variety of advanced nanoscale biological applications.

  10. Electrochemical enzymatic biosensors using carbon nanofiber nanoelectrode arrays

    NASA Astrophysics Data System (ADS)

    Li, Jun; Li, Yi-fen; Swisher, Luxi Z.; Syed, Lateef U.; Prior, Allan M.; Nguyen, Thu A.; Hua, Duy H.

    2012-10-01

    The reduction of electrode size down to nanometers could dramatically enhance detection sensitivity and temporal resolution. Nanoelectrode arrays (NEAs) are of particular interest for ultrasensitive biosensors. Here we report the study of two types of biosensors for measuring enzyme activities using NEAs fabricated with vertically aligned carbon nanofibers (VACNFs). VACNFs of ~100 nm in average diameter and 3-5 μm in length were grown on conductive substrates as uniform vertical arrays which were then encapsulated in SiO2 matrix leaving only the tips exposed. We demonstrate that such VACNF NEAs can be used in profiling enzyme activities through monitoring the change in electrochemical signals induced by enzymatic reactions to the peptides attached to the VACNF tip. The cleavage of the tetrapeptide with a ferrocene tag by a cancerrelated protease (legumain) was monitored with AC voltammetry. Real-time electrochemical impedance spectroscopy (REIS) was used for fast label-free detection of two reversible processes, i.e. phosphorylation by c-Src tyrosine kinase and dephosphorylation by protein tyrosine phosphatase 1B (PTP1B). The REIS data of phosphorylation were slow and unreliable, but those of dephosphorylation showed large and fast exponential decay due to much higher activity of phosphatase PTP1B. The kinetic data were analyzed with a heterogeneous Michaelis-Menten model to derive the "specificity constant" kcat/Km, which is 8.2x103 M-1s-1 for legumain and (2.1 ± 0.1) x 107 M-1s-1 for phosphatase (PTP1B), well consistent with literature. It is promising to develop VACNF NEA based electrochemical enzymatic biosensors as portable multiplex electronic techniques for rapid cancer diagnosis and treatment monitoring.

  11. Strong and stiff aramid nanofiber/carbon nanotube nanocomposites.

    PubMed

    Zhu, Jiaqi; Cao, Wenxin; Yue, Mingli; Hou, Ying; Han, Jiecai; Yang, Ming

    2015-03-24

    Small but strong carbon nanotubes (CNTs) are fillers of choice for composite reinforcement owing to their extraordinary modulus and strength. However, the mechanical properties of the nanocomposites are still much below those for mechanical parameters of individual nanotubes. The gap between the expectation and experimental results arises not only from imperfect dispersion and poor load transfer but also from the unavailability of strong polymers that can be effectively utilized within the composites of nanotubes. Aramid nanofibers (ANFs) with analogous morphological features to nanotubes represent a potential choice to complement nanotubes given their intrinsic high mechanical performance and the dispersible nature, which enables solvent-based processing methods. In this work, we showed that composite films made from ANFs and multiwalled CNTs (MWCNTs) by vacuum-assisted flocculation and vacuum-assisted layer-by-layer assembly exhibited high ultimate strength of up to 383 MPa and Young's modulus (stiffness) of up to 35 GPa, which represent the highest values among all the reported random CNT nanocomposites. Detailed studies using different imaging and spectroscopic characterizations suggested that the multiple interfacial interactions between nanotubes and ANFs including hydrogen bonding and π-π stacking are likely the key parameters responsible for the observed mechanical improvement. Importantly, our studies further revealed the attractive thermomechanical characteristics of these nanocomposites with high thermal stability (up to 520 °C) and ultralow coefficients of thermal expansion (2-6 ppm·K(-1)). Our results indicated that ANFs are promising nanoscale building blocks for functional ultrastrong and stiff materials potentially extendable to nanocomposites based on other nanoscale fillers. PMID:25712334

  12. A novel methanol sensor based on gas-penetration through a porous polypyrrole-coated polyacrylonitrile nanofiber mat.

    PubMed

    Jun, Tae-Sun; Ho, Thi Anh; Rashid, Muhammad; Kim, Yong Shin

    2013-09-01

    In this work, we propose a novel chemoresistive gas sensor operated under a vertical analyte flow passing through a permeable sensing membrane. Such a configuration is different from the use of a planar sensor implemented under a conventional horizontal flow. A highly porous core-shell polyacrylonitrile-polypyrrole (PAN@PPy) nanofiber mat was prepared as the sensing element via electrospinning and two-step vapor-phase polymerization (VPP). Various analysis methods such as SEM, TEM, FT-IR and XPS measurements were employed in order to characterize structural features of the porous sensing mat. These analyses confirmed that very thin (ca. 10 nm) conductive PPy sheath layers were deposited by VPP on electrospun PAN nanofibers with an average diameter of 258 nm. Preliminary results revealed that the gas penetration-type PAN@PPy sensor had a higher sensor response and shorter detection and recovery times upon exposure to methanol analyte when compared with a conventional horizontal flow sensor due to efficient and fast analyte transfer into the sensing layer. PMID:24205639

  13. Theoretical and practical aspects of chemical functionalization of carbon nanofibers (CNFs): DFT calculations and adsorption study.

    PubMed

    Rokhina, Ekaterina V; Lahtinen, Manu; Makarova, Katerina; Jegatheesan, Veeriah; Virkutyte, Jurate

    2012-06-01

    The nitric acid-functionalized commercial carbon nanofibers (CNFs) were comprehensively studied by instrumental (XRD, BET, SEM, TGA) and theoretical (DFT calculations) methods. The detailed surface study revealed the variation in the characteristics of functionalized CNFs, such as a decreased (up to 34%) surface area and impacted structural, electronic and chemical properties. The effects of functional groups were studied by comparison with pristine nanofibers. The results showed that the C-C bond lengths of the modified CNFs varied significantly. Chemical functionalization altered the frontier orbitals of the pristine material, and therefore altered the nature of their interactions with other substances. Moreover, the pristine and modified CNFs were tested for the removal of phenol from aqueous solutions. It was observed that surface modification tuned the adsorption capacity of carbon nanofibers (up to 0.35 mmol g(-1)), whereas original fibers did not demonstrate any adsorption capacity of phenol. PMID:22209137

  14. Electrospun carbon nanofibers for improved electrical conductivity of fiber reinforced composites

    NASA Astrophysics Data System (ADS)

    Alarifi, Ibrahim M.; Alharbi, Abdulaziz; Khan, Waseem S.; Asmatulu, Ramazan

    2015-04-01

    Polyacrylonitrile (PAN) was dissolved in dimethylformamide (DMF), and then electrospun to generate nanofibers using various electrospinning conditions, such as pump speeds, DC voltages and tip-to-collector distances. The produced nanofibers were oxidized at 270 °C for 1 hr, and then carbonized at 850 °C in an argon gas for additional 1 hr. The resultant carbonized PAN nanofibers were placed on top of the pre-preg carbon fiber composites as top layers prior to the vacuum oven curing following the pre-preg composite curing procedures. The major purpose of this study is to determine if the carbonized nanofibers on the fiber reinforced composites can detect the structural defects on the composite, which may be useful for the structural health monitoring (SHM) of the composites. Scanning electron microscopy images showed that the electrospun PAN fibers were well integrated on the pre-preg composites. Electrical conductivity studies under various tensile loads revealed that nanoscale carbon fibers on the fiber reinforced composites detected small changes of loads by changing the resistance values. Electrically conductive composite manufacturing can have huge benefits over the conventional composites primarily used for the military and civilian aircraft and wind turbine blades.

  15. Carbon functionalized TiO2 nanofibers for high efficiency photocatalysis

    NASA Astrophysics Data System (ADS)

    Raghava Reddy, Kakarla; Gomes, Vincent G.; Hassan, Mahbub

    2014-03-01

    TiO2 nanofibers (30-50 nm diameter), fabricated by the electro-spinning process, were modified with organo-silane agents via a coupling reaction and were grafted with carbohydrate molecules. The mixture was carbonized to produce a uniform coating of amorphous carbon on the surface of the TiO2 nanofibers. The TiO2@C nanofibers were characterized by high resolution electron microscopy (HRTEM), x-ray diffraction (XRD), x-ray photoelectron (XPS), Fourier transform infrared (FTIR) and UV-vis spectroscopy. The photocatalytic property of the functional TiO2 and carbon nanocomposite was tested via the decomposition of an organic pollutant. The catalytic activity of the covalently functionalized nanocomposite was found to be significantly enhanced in comparison to unfunctionalized composite and pristine TiO2 due to the synergistic effect of nanostructured TiO2 and amorphous carbon bound via covalent bonds. The improvement in performance is due to bandgap modification in the 1D co-axial nanostructure where the anatase phase is bound by nano-carbon, providing a large surface to volume ratio within a confined space. The superior photocatalytic performance and recyclability of 1D TiO2@C nanofiber composites for water purification were established through dye degradation experiments.

  16. Fischer-Tropsch synthesis on hierarchically structured cobalt nanoparticle/carbon nanofiber/carbon felt composites.

    PubMed

    Zarubova, Sarka; Rane, Shreyas; Yang, Jia; Yu, Yingda; Zhu, Ye; Chen, De; Holmen, Anders

    2011-07-18

    The hierarchically structured carbon nanofibers (CNFs)/carbon felt composites, in which CNFs were directly grown on the surface of microfibers in carbon felt, forming a CNF layer on a micrometer range that completely covers the microfiber surfaces, were tested as a novel support material for cobalt nanoparticles in the highly exothermic Fischer-Tropsch (F-T) synthesis. A compact, fixed-bed reactor, made of disks of such composite materials, offered the advantages of improved heat and mass transfer, relatively low pressure drop, and safe handling of immobilized CNFs. An efficient 3-D thermal conductive network in the composite provided a relatively uniform temperature profile, whereas the open structure of the CNF layer afforded an almost 100 % effectiveness of Co nanoparticles in the F-T synthesis in the fixed bed. The greatly improved mass and heat transport makes the compact reactor attractive for applications in the conversion of biomass, coal, and natural gas to liquids. PMID:21563315

  17. One-step catalytic growth of carbon nanofiber arrays vertically aligned on carbon substrate

    SciTech Connect

    Li, Xun; State Key Laboratory of Soil and Sustainable Agriculture, Institute of Soil Science, Chinese Academy of Sciences, Nanjing 210008 ; Xu, Zheng

    2012-06-15

    Highlights: ► Acetylene as carbon resource and copper foil as catalyst. ► Three carbon nanostructures are synthesized by modulating feeding gas compositions. ► NH{sub 3} is a key factor in the growth of VA-CNF arrays. -- Abstract: Vertically aligned carbon nanofiber (VA-CNF) arrays on carbon substrate have been synthesized via one-step chemical vapor deposition process on copper foil, by using acetylene as carbon resource. Three types of carbon nanostructures, viz. bare carbon films, CNFs and VA-CNFs grown on carbon substrate, could be selectively synthesized by only modulating the concentration of C{sub 2}H{sub 2} and NH{sub 3} in the feeding gases. It was found that NH{sub 3} was a key factor in the growth of VA-CNF arrays, which could increase the diffusion capability of copper atoms in carbon materials, therefore promote forming larger spherical Cu NPs catalysts for the growth of VA-CNFs. Furthermore, a growth mechanism in different feeding gas compositions was proposed.

  18. Remarkable improvement in microwave absorption by cloaking a micro-scaled tetrapod hollow with helical carbon nanofibers.

    PubMed

    Jian, Xian; Chen, Xiangnan; Zhou, Zuowan; Li, Gang; Jiang, Man; Xu, Xiaoling; Lu, Jun; Li, Qiming; Wang, Yong; Gou, Jihua; Hui, David

    2015-02-01

    Helical nanofibers are prepared through in situ growth on the surface of a tetrapod-shaped ZnO whisker (T-ZnO), by employing a precursor decomposition method then adding substrate. After heat treatment at 900 °C under argon, this new composite material, named helical nanofiber-T-ZnO, undergoes a significant change in morphology and structure. The T-ZnO transforms from a solid tetrapod ZnO to a micro-scaled tetrapod hollow carbon film by reduction of the organic fiber at 900 °C. Besides, helical carbon nanofibers, generated from the carbonization of helical nanofibers, maintain the helical morphology. Interestingly, HCNFs with the T-hollow exhibit remarkable improvement in electromagnetic wave loss compared with the pure helical nanofibers. The enhanced loss ability may arise from the efficient dielectric friction, interface effect in the complex nanostructures and the micro-scaled tetrapod-hollow structure. PMID:25510199

  19. Flame Synthesis Of Single-Walled Carbon Nanotubes And Nanofibers

    NASA Technical Reports Server (NTRS)

    Wal, Randy L. Vander; Berger, Gordon M.; Ticich, Thomas M.

    2003-01-01

    Carbon nanotubes are widely sought for a variety of applications including gas storage, intercalation media, catalyst support and composite reinforcing material [1]. Each of these applications will require large scale quantities of CNTs. A second consideration is that some of these applications may require redispersal of the collected CNTs and attachment to a support structure. If the CNTs could be synthesized directly upon the support to be used in the end application, a tremendous savings in post-synthesis processing could be realized. Therein we have pursued both aerosol and supported catalyst synthesis of CNTs. Given space limitations, only the aerosol portion of the work is outlined here though results from both thrusts will be presented during the talk. Aerosol methods of SWNT, MWNT or nanofiber synthesis hold promise of large-scale production to supply the tonnage quantities these applications will require. Aerosol methods may potentially permit control of the catalyst particle size, offer continuous processing, provide highest product purity and most importantly, are scaleable. Only via economy of scale will the cost of CNTs be sufficient to realize the large-scale structural and power applications on both earth and in space. Present aerosol methods for SWNT synthesis include laser ablation of composite metalgraphite targets or thermal decomposition/pyrolysis of a sublimed or vaporized organometallic [2]. Both approaches, conducted within a high temperature furnace, have produced single-walled nanotubes (SWNTs). The former method requires sophisticated hardware and is inherently limited by the energy deposition that can be realized using pulsed laser light. The latter method, using expensive organometallics is difficult to control for SWNT synthesis given a range of gasparticle mixing conditions along variable temperature gradients; multi-walled nanotubes (MWNTs) are a far more likely end products. Both approaches require large energy expenditures and

  20. "Covalent functionalization and electron-transfer properties of vertically aligned carbon nanofibers: The importance of edge-plane sites"

    SciTech Connect

    Landis, Elizabeth; Klein, Kate; Albert, Liao; Pop, Eric; Hensley, Dale K; Melechko, Anatoli; Hamers, Robert

    2010-01-01

    The use of covalently bonded molecular layers provides a way to combine the outstanding stability and electrochemical properties of carbon-based structures with the unique properties of molecular structures for applications such as electrocatalysis and solar conversion. The functionalization of vertically aligned carbon nanofibers (VACNFs) with 1-alkenes, using ultraviolet light, was investigated as a potential way to impart a variety of different functional groups onto the nanofiber sidewalls. We report how variations in the nanofiber growth rate impact both the amount of exposed edge-plane sites and the resulting electrochemical activity toward Ru(NH{sub 3}){sub 6}{sup 3+/2+} and Fe(CN){sub 6}{sup 3-/4-} redox couples. Measurements of the distribution of surface oxides show that surface oxides are unaffected by the grafting of alkenes to the nanofibers. Carbon nanofiber reactivity was also compared to multiwalled and single-walled carbon nanotubes. Our results demonstrate that edge-plane sites are preferred sites for photochemical grafting, but that the grafting of molecular layers only slightly reduces the overall electrochemical activity of the nanofibers toward the Ru(NH{sub 3}){sub 6}{sup 3+/2+} couple. These results provide new insights into the relationships between the chemical reactivity and electrochemical properties of nanostructured carbon materials and highlight the crucial role that exposed edge-plane sites play in the electrochemical properties of carbon nanotubes and nanofibers.

  1. Carbothermal transformation of a graphitic carbon nanofiber/silica aerogel composite to a SiC/silica nanocomposite.

    PubMed

    Lu, Weijie; Steigerwalt, Eve S; Moore, Joshua T; Sullivan, Lisa M; Collins, W Eugene; Lukehart, C M

    2004-09-01

    Carbon nanofiber/silica aerogel composites are prepared by sol-gel processing of surface-enhanced herringbone graphitic carbon nanofibers (GCNF) and Si(OMe)4, followed by supercritical CO2 drying. Heating the resulting GCNF/silica aerogel composites to 1650 degrees C under a partial pressure of Ar gas initiates carbothermal reaction between the silica aerogel matrix and the carbon nanofiber component to form SiC/silica nanocomposites. The SiC phase is present as nearly spherical nanoparticles, having an average diameter of ca. 8 nm. Formation of SiC is confirmed by powder XRD and by Raman spectroscopy. PMID:15570963

  2. Egg-Box Structure in Cobalt Alginate: A New Approach to Multifunctional Hierarchical Mesoporous N-Doped Carbon Nanofibers for Efficient Catalysis and Energy Storage

    PubMed Central

    2015-01-01

    Carbon nanomaterials with both doped heteroatom and porous structure represent a new class of carbon nanostructures for boosting electrochemical application, particularly sustainable electrochemical energy conversion and storage applications. We herein demonstrate a unique large-scale sustainable biomass conversion strategy for the synthesis of earth-abundant multifunctional carbon nanomaterials with well-defined doped heteroatom level and multimodal pores through pyrolyzing electrospinning renewable natural alginate. The key part for our chemical synthesis is that we found that the egg-box structure in cobalt alginate nanofiber can offer new opportunity to create large mesopores (∼10–40 nm) on the surface of nitrogen-doped carbon nanofibers. The as-prepared hierarchical carbon nanofibers with three-dimensional pathway for electron and ion transport are conceptually new as high-performance multifunctional electrochemical materials for boosting the performance of oxygen reduction reaction (ORR), lithium ion batteries (LIBs), and supercapacitors (SCs). In particular, they show amazingly the same ORR activity as commercial Pt/C catalyst and much better long-term stability and methanol tolerance for ORR than Pt/C via a four-electron pathway in alkaline electrolyte. They also exhibit a large reversible capacity of 625 mAh g–1 at 1 A g–1, good rate capability, and excellent cycling performance for LIBs, making them among the best in all the reported carbon nanomaterials. They also represent highly efficient carbon nanomaterials for SCs with excellent capacitive behavior of 197 F g–1 at 1 A g–1 and superior stability. The present work highlights the importance of biomass-derived multifunctional mesoporous carbon nanomaterials in enhancing electrochemical catalysis and energy storage. PMID:27162980

  3. Egg-Box Structure in Cobalt Alginate: A New Approach to Multifunctional Hierarchical Mesoporous N-Doped Carbon Nanofibers for Efficient Catalysis and Energy Storage.

    PubMed

    Li, Daohao; Lv, Chunxiao; Liu, Long; Xia, Yanzhi; She, Xilin; Guo, Shaojun; Yang, Dongjiang

    2015-08-26

    Carbon nanomaterials with both doped heteroatom and porous structure represent a new class of carbon nanostructures for boosting electrochemical application, particularly sustainable electrochemical energy conversion and storage applications. We herein demonstrate a unique large-scale sustainable biomass conversion strategy for the synthesis of earth-abundant multifunctional carbon nanomaterials with well-defined doped heteroatom level and multimodal pores through pyrolyzing electrospinning renewable natural alginate. The key part for our chemical synthesis is that we found that the egg-box structure in cobalt alginate nanofiber can offer new opportunity to create large mesopores (∼10-40 nm) on the surface of nitrogen-doped carbon nanofibers. The as-prepared hierarchical carbon nanofibers with three-dimensional pathway for electron and ion transport are conceptually new as high-performance multifunctional electrochemical materials for boosting the performance of oxygen reduction reaction (ORR), lithium ion batteries (LIBs), and supercapacitors (SCs). In particular, they show amazingly the same ORR activity as commercial Pt/C catalyst and much better long-term stability and methanol tolerance for ORR than Pt/C via a four-electron pathway in alkaline electrolyte. They also exhibit a large reversible capacity of 625 mAh g(-1) at 1 A g(-1), good rate capability, and excellent cycling performance for LIBs, making them among the best in all the reported carbon nanomaterials. They also represent highly efficient carbon nanomaterials for SCs with excellent capacitive behavior of 197 F g(-1) at 1 A g(-1) and superior stability. The present work highlights the importance of biomass-derived multifunctional mesoporous carbon nanomaterials in enhancing electrochemical catalysis and energy storage. PMID:27162980

  4. DC Plasma Synthesis of Vertically Aligned Carbon Nanofibers for Biointerfacing

    NASA Astrophysics Data System (ADS)

    Pearce, Ryan Christopher

    Vertically aligned carbon nanofibers (VACNFs) are a class of materials whose nanoscale dimensions and physical properties makes them uniquely suitable as functional elements in many applications for biodetection and biointerfacing on a cellular level. Control of VACNF synthesis by catalytic plasma enhanced chemical vapor deposition (PECVD) presents many challenges in integration into devices and structures designed for biointerfacing, such as transparent or flexible substrates. This dissertation addresses ways to overcome many of these issues in addition to deepening the fundamental understanding of nano-synthesis in catalytic PECVD. First, a survey of the field of VACNF synthesis and biointerfacing is presented, identifying the present challenges and greatest experimental applications. It is followed by experimental observations that elucidate the underlying mechanism to fiber alignment during synthesis, a critical step for deterministic control of fiber growth. Using a grid of electrodes patterned by photolithography on an insulating substrate, it was found that the alignment of the fibers is controlled by the anisotropic etching provided by ions during dc-PECVD synthesis. The VACNFs that have been utilized for many cellular interfacing experiments have unique mechanical and fluorescent properties due to a SiNx coating. The mechanism for SiNx deposition to VACNF sidewalls during synthesis is explored in addition to a detailed study of the optical properties of the coating. To explain the optical properties of this coating it is proposed that the source of photoluminescence for the SiNx coated VACNFs is quantum confinement effects due to the presence of silicon nanoclusters embedded in a Si3N4 matrix. These luminescent fibers have proven useful as registry markers in cell impalefection studies. To realize VACNF arrays used as an inflatable angioplasty balloon with embedded fibers to deliver drugs across the blood-brain barrier, a method for transferring fibers to

  5. Elastic and hierarchical porous carbon nanofibrous membranes incorporated with NiFe2O4 nanocrystals for highly efficient capacitive energy storage.

    PubMed

    Ge, Jianlong; Fan, Gang; Si, Yang; He, Jianxin; Kim, Hak-Yong; Ding, Bin; Al-Deyab, Salem S; El-Newehy, Mohamed; Yu, Jianyong

    2016-01-28

    Flexible membranes created from porous carbon nanofibers (CNFs) hold great promise in the next generation wearable energy storage devices, but challenges still remain due to the poor mechanical properties of porous carbon nanofibers. Here, we report a facile strategy to fabricate elastic and hierarchical porous CNF membranes with NiFe2O4 nanocrystals embedded via multicomponent electrospinning and nano-doping methods. Benefiting from the scattering effect of NiFe2O4 nanocrystals and graphitized carbon layers for the condensed stress, the resultant CNF membranes exhibit an enhanced elasticity with a bending radius <12 μm, rapid recovery from the deformations, and a superior softness. Quantitative pore size distribution and fractal analysis reveal that the CNFs possessed tunable porous structures with a high surface area of 493 m(2) g(-1) and a pore volume of 0.31 cm(3) g(-1). Benefiting from the robust mechanical stability, hierarchical porous structures and good electrochemical properties, the NiFe2O4 doped CNF membranes demonstrate a high electrical capacitance of 343 F g(-1), and good reversibility with a cycling efficiency of 97.4% even after 10,000 cycles. The successful synthesis of elastic porous CNF membranes also provided a versatile platform for the design and development of functional CNF based materials for various applications. PMID:26731700

  6. Use of facile mechanochemical method to functionalize carbon nanofibers with nanostructured polyaniline and their electrochemical capacitance

    PubMed Central

    2012-01-01

    A facile approach to functionalize carbon nanofibers [CNFs] with nanostructured polyaniline was developed via in situ mechanochemical polymerization of polyaniline in the presence of chemically treated CNFs. The nanostructured polyaniline grafting on the CNF was mainly in a form of branched nanofibers as well as rough nanolayers. The good dispersibility and processability of the hybrid nanocomposite could be attributed to its overall nanostructure which enhanced its accessibility to the electrolyte. The mechanochemical oxidation polymerization was believed to be related to the strong Lewis acid characteristic of FeCl3 and the Lewis base characteristic of aniline. The growth mechanism of the hierarchical structured nanofibers was also discussed. After functionalization with the nanostructured polyaniline, the hybrid polyaniline/CNF composite showed an enhanced specific capacitance, which might be related to its hierarchical nanostructure and the interaction between the aromatic polyaniline molecules and the CNFs. PMID:22315992

  7. Polyaniline nanofiber/large mesoporous carbon composites as electrode materials for supercapacitors

    NASA Astrophysics Data System (ADS)

    Liu, Huan; Xu, Bin; Jia, Mengqiu; Zhang, Mei; Cao, Bin; Zhao, Xiaonan; Wang, Yu

    2015-03-01

    A composite of polyaniline nanofiber/large mesoporous carbon (PANI-F/LMC) hybrid was prepared by an in situ chemical oxidative polymerization of aniline monomer with nano-CaCO3 templated LMC as host matrix for supercapacitors. The morphology, composition and electronic structure of the composites (PANI-F/LMC) together with pure PANI nanofibers and the LMC were characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), FT-IR, X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS). It is found that the PANI nanofibers were incorporated into the large mesochannels of LMC with interpenetrating framework formed. Such unique structure endows the PANI-F/LMC composite with a high capacitance of 473 F g-1 at a current load of 0.1 A g-1 with good rate performance and cycling stability, suggesting its potential application in the electrode material for supercapacitors.

  8. Use of facile mechanochemical method to functionalize carbon nanofibers with nanostructured polyaniline and their electrochemical capacitance

    NASA Astrophysics Data System (ADS)

    Du, Xusheng; Liu, Hong-Yuan; Cai, Guipeng; Mai, Yiu-Wing; Baji, Avinash

    2012-02-01

    A facile approach to functionalize carbon nanofibers [CNFs] with nanostructured polyaniline was developed via in situ mechanochemical polymerization of polyaniline in the presence of chemically treated CNFs. The nanostructured polyaniline grafting on the CNF was mainly in a form of branched nanofibers as well as rough nanolayers. The good dispersibility and processability of the hybrid nanocomposite could be attributed to its overall nanostructure which enhanced its accessibility to the electrolyte. The mechanochemical oxidation polymerization was believed to be related to the strong Lewis acid characteristic of FeCl3 and the Lewis base characteristic of aniline. The growth mechanism of the hierarchical structured nanofibers was also discussed. After functionalization with the nanostructured polyaniline, the hybrid polyaniline/CNF composite showed an enhanced specific capacitance, which might be related to its hierarchical nanostructure and the interaction between the aromatic polyaniline molecules and the CNFs.

  9. Enhancing capacitive deionization performance of electrospun activated carbon nanofibers by coupling with carbon nanotubes.

    PubMed

    Dong, Qiang; Wang, Gang; Wu, Tingting; Peng, Senpei; Qiu, Jieshan

    2015-05-15

    Capacitive deionization (CDI) is an alternative, effective and environmentally friendly technology for desalination of brackish water. The performance of the CDI device is highly determined by the electrode materials. In this paper, a composite of carbon nanotubes (CNTs) embedded in activated carbon nanofiber (ACF) was prepared by a direct co-electrospinning way and subsequent CO2 activation. The introduction of CNTs can greatly improve the conductivity while the CO2-mediated activation can render the final product with high porosity. As such, the hybrid structure can provide an excellent storage space and pathways for ion adsorption and conduction. When evaluated as electrode materials for CDI, the as-prepared CNT/ACF composites with higher electrical conductivity and mesopore ratios exhibited higher electrosorption capacity and good regeneration performance in comparison with the pure ACF. PMID:25595622

  10. Carbon Nanotubes-Adsorbed Electrospun PA66 Nanofiber Bundles with Improved Conductivity and Robust Flexibility.

    PubMed

    Guan, Xiaoyang; Zheng, Guoqiang; Dai, Kun; Liu, Chuntai; Yan, Xingru; Shen, Changyu; Guo, Zhanhu

    2016-06-01

    Electrospun polyamide (PA) 66 nanofiber bundles with high conductivity, improved strength, and robust flexibility were successfully manufactured through simply adsorbing multiwall carbon nanotubes (MWNTs) on the surface of electrospun PA66 nanofibers. The highest electrical conductivity (0.2 S/cm) and tensile strength (103.3 MPa) were achieved for the bundles immersed in the suspension with 0.05 wt % MWNTs, indicating the formation of conductive network from adsorbed MWNTs on the surface of PA66 nanofibers. The decrease of porosity for the bundles immersed in the MWNT dispersion and the formation of hydrogen bond between PA66 nanofibers and MWNTs suggest a superb interfacial interaction, which is responsible for the excellent mechanical properties of the nanocomposite bundles. Furthermore, the resistance fluctuation under bending is less than 3.6%, indicating a high flexibility of the nanocomposite bundles. The resistance of the nanocomposite bundle had a better linear dependence on the temperature applied between 30 and 150 °C. More importantly, such highest working temperature of 150 °C far exceeded that of other polymer-based temperature sensors previously reported. This suggests that such prepared MWNTs-adsorbed electrospun PA66 nanofiber bundles have great potentials in high temperature detectors. PMID:27172292

  11. Ultrasensitive, Label Free, Chemiresistive Nanobiosensor Using Multiwalled Carbon Nanotubes Embedded Electrospun SU-8 Nanofibers.

    PubMed

    Durga Prakash, Matta; Vanjari, Siva Rama Krishna; Sharma, Chandra Shekhar; Singh, Shiv Govind

    2016-01-01

    This paper reports the synthesis and fabrication of aligned electrospun nanofibers derived out of multiwalled carbon nanotubes (MWCNTs) embedded SU-8 photoresist, which are targeted towards ultrasensitive biosensor applications. The ultrasensitivity (detection in the range of fg/mL) and the specificity of these biosensors were achieved by complementing the inherent advantages of MWCNTs such as high surface to volume ratio and excellent electrical and transduction properties with the ease of surface functionalization of SU-8. The electrospinning process was optimized to precisely align nanofibers in between two electrodes of a copper microelectrode array. MWCNTs not only enhance the conductivity of SU-8 nanofibers but also act as transduction elements. In this paper, MWCNTs were embedded way beyond the percolation threshold and the optimum percentage loading of MWCNTs for maximizing the conductivity of nanofibers was figured out experimentally. As a proof of concept, the detection of myoglobin, an important biomarker for on-set of Acute Myocardial Infection (AMI) has been demonstrated by functionalizing the nanofibers with anti-myoglobin antibodies and carrying out detection using a chemiresistive method. This simple and robust device yielded a detection limit of 6 fg/mL. PMID:27563905

  12. Influence of oxygen on nitrogen-doped carbon nanofiber growth directly on nichrome foil.

    PubMed

    Vishwakarma, Riteshkumar; Shinde, Sachin M; Rosmi, Mohamad Saufi; Takahashi, Chisato; Papon, Remi; Mahyavanshi, Rakesh D; Ishii, Yosuke; Kawasaki, Shinji; Kalita, Golap; Tanemura, Masaki

    2016-09-01

    The synthesis of various nitrogen-doped (N-doped) carbon nanostructures has been significantly explored as an alternative material for energy storage and metal-free catalytic applications. Here, we reveal a direct growth technique of N-doped carbon nanofibers (CNFs) on flexible nichrome (NiCr) foil using melamine as a solid precursor. Highly reactive Cr plays a critical role in the nanofiber growth process on the metal alloy foil in an atmospheric pressure chemical vapor deposition (APCVD) process. Oxidation of Cr occurs in the presence of oxygen impurities, where Ni nanoparticles are formed on the surface and assist the growth of nanofibers. Energy-dispersive x-ray spectroscopy (EDXS) and x-ray photoelectron spectroscopy (XPS) clearly show the transformation process of the NiCr foil surface with annealing in the presence of oxygen impurities. The structural change of NiCr foil assists one-dimensional (1D) CNF growth, rather than the lateral two-dimensional (2D) growth. The incorporation of distinctive graphitic and pyridinic nitrogen in the graphene lattice are observed in the synthesized nanofiber, owing to better nitrogen solubility. Our finding shows an effective approach for the synthesis of highly N-doped carbon nanostructures directly on Cr-based metal alloys for various applications. PMID:27479000

  13. Influence of oxygen on nitrogen-doped carbon nanofiber growth directly on nichrome foil

    NASA Astrophysics Data System (ADS)

    Vishwakarma, Riteshkumar; Shinde, Sachin M.; Saufi Rosmi, Mohamad; Takahashi, Chisato; Papon, Remi; Mahyavanshi, Rakesh D.; Ishii, Yosuke; Kawasaki, Shinji; Kalita, Golap; Tanemura, Masaki

    2016-09-01

    The synthesis of various nitrogen-doped (N-doped) carbon nanostructures has been significantly explored as an alternative material for energy storage and metal-free catalytic applications. Here, we reveal a direct growth technique of N-doped carbon nanofibers (CNFs) on flexible nichrome (NiCr) foil using melamine as a solid precursor. Highly reactive Cr plays a critical role in the nanofiber growth process on the metal alloy foil in an atmospheric pressure chemical vapor deposition (APCVD) process. Oxidation of Cr occurs in the presence of oxygen impurities, where Ni nanoparticles are formed on the surface and assist the growth of nanofibers. Energy-dispersive x-ray spectroscopy (EDXS) and x-ray photoelectron spectroscopy (XPS) clearly show the transformation process of the NiCr foil surface with annealing in the presence of oxygen impurities. The structural change of NiCr foil assists one-dimensional (1D) CNF growth, rather than the lateral two-dimensional (2D) growth. The incorporation of distinctive graphitic and pyridinic nitrogen in the graphene lattice are observed in the synthesized nanofiber, owing to better nitrogen solubility. Our finding shows an effective approach for the synthesis of highly N-doped carbon nanostructures directly on Cr-based metal alloys for various applications.

  14. Ultrafine Mo2C nanoparticles encapsulated in N-doped carbon nanofibers with enhanced lithium storage performance.

    PubMed

    Li, Ruirui; Wang, Shuguang; Wang, Wei; Cao, Minhua

    2015-10-14

    Rechargeable lithium ion batteries (LIBs) have attracted extensive attention globally due to their good cycling stability, high energy density, and rapid-rate capability, while the rational design of electrode materials can significantly improve their electrochemical performance. In this work, ultrafine Mo2C nanoparticles (NPs) were successfully encapsulated in one dimensional (1D) N-doped porous carbon nanofibers to form a hybrid (Mo2C-NCNFs) through a single-nozzle electrospinning approach coupled with post-pyrolysis. The sizes of the Mo2C NPs were in the range of 2-4 nm and the ultrafine Mo2C NPs were uniformly encapsulated in the N-doped carbon nanofibers forming a highly conductive and interconnecting network, which can facilitate fast electronic transport. When evaluated as an anode material for LIBs, the resultant hybrid exhibits stable cycling performance and excellent rate behavior. More remarkably, the Mo2C-NCNFs hybrid is capable of delivering a specific capacity of 658.0 mA h g(-1) under 100 mA g(-1) after 50 cycles. Even under 2000 mA g(-1), a relatively high specific capacity of 411.9 mA h g(-1) can be achieved, which surpasses the theoretical capacity of graphite (372 mA h g(-1)). The excellent lithium storage performance can be attributed to its unique nanostructure with a strong interaction between the ultrafine Mo2C NPs and N-doped carbon that effectively tolerates the volume change, suppresses the agglomeration of Mo2C NPs, and provides conductive pathways for highly efficient charge transfer during lithium insertion and extraction. PMID:26344047

  15. Carbon nanofiber mesoporous films: efficient platforms for bio-hydrogen oxidation in biofuel cells.

    PubMed

    de Poulpiquet, Anne; Marques-Knopf, Helena; Wernert, Véronique; Giudici-Orticoni, Marie Thérèse; Gadiou, Roger; Lojou, Elisabeth

    2014-01-28

    The discovery of oxygen and carbon monoxide tolerant [NiFe] hydrogenases was the first necessary step toward the definition of a novel generation of hydrogen fed biofuel cells. The next important milestone is now to identify and overcome bottlenecks limiting the current densities, hence the power densities. In the present work we report for the first time a comprehensive study of herringbone carbon nanofiber mesoporous films as platforms for enhanced biooxidation of hydrogen. The 3D network allows mediatorless hydrogen oxidation by the membrane-bound hydrogenase from the hyperthermophilic bacterium Aquifex aeolicus. We investigate the key physico-chemical parameters that enhance the catalytic efficiency, including surface chemistry and hierarchical porosity of the biohybrid film. We also emphasize that the catalytic current is limited by mass transport inside the mesoporous carbon nanofiber film. Provided hydrogen is supplied inside the carbon film, the combination of the hierarchical porosity of the carbon nanofiber film with the hydrophobicity of the treated carbon material results in very high efficiency of the bioelectrode. By optimization of the whole procedure, current densities as high as 4.5 mA cm(-2) are reached with a turnover frequency of 48 s(-1). This current density is almost 100 times higher than when hydrogenase is simply adsorbed at a bare graphite electrode, and more than 5 times higher than the average of the previous reported current densities at carbon nanotube modified electrodes, suggesting that carbon nanofibers can be efficiently used in future sustainable H2/O2 biofuel cells. PMID:24296569

  16. Synthesis of Porous NiO and ZnO Submicro- and Nanofibers from Electrospun Polymer Fiber Templates

    NASA Astrophysics Data System (ADS)

    Qiu, Yejun; Yu, Jie; Zhou, Xiaosong; Tan, Cuili; Yin, Jing

    2009-02-01

    Porous nickel oxide (NiO) and zinc oxide (ZnO) submicro- and nanofibers were synthesized by impregnating electrospun polyacrylonitrile (PAN) fiber templates with corresponding metal nitrate aqueous solutions and subsequent calcination. The diameter of the NiO and ZnO fibers was closely related to that of the template fibers and larger diameters were obtained when using the template fibers with larger diameter. SEM results showed that the NiO and ZnO fibers have a large amount of pores with diameters ranging from 5 nm to 20 nm and 50 nm to 100 nm, respectively. Energy dispersive X-ray (EDX) spectra and X-ray diffraction (XRD) patterns testified that the obtained materials were NiO and ZnO with high purity.

  17. Carbon nanofibers grafted on activated carbon as an electrode in high-power supercapacitors.

    PubMed

    Gryglewicz, Grażyna; Śliwak, Agata; Béguin, François

    2013-08-01

    A hybrid electrode material for high-power supercapacitors was fabricated by grafting carbon nanofibers (CNFs) onto the surface of powdered activated carbon (AC) through catalytic chemical vapor deposition (CCVD). A uniform thin layer of disentangled CNFs with a herringbone structure was deposited on the carbon surface through the decomposition of propane at 450 °C over an AC-supported nickel catalyst. CNF coating was controlled by the reaction time and the nickel content. The superior CNF/AC composite displays excellent electrochemical performance in a 0.5 mol L(-1) solution of K2 SO4 due to its unique structure. At a high scan rate (100 mV s(-1) ) and current loading (20 A g(-1) ), the capacitance values were three- and fourfold higher than those for classical AC/carbon black composites. Owing to this feature, a high energy of 10 Wh kg(-1) was obtained over a wide power range in neutral medium at a voltage of 0.8 V. The significant enhancement of charge propagation is attributed to the presence of herringbone CNFs, which facilitate the diffusion of ions in the electrode and play the role of electronic bridges between AC particles. An in situ coating of AC with short CNFs (below 200 nm) is a very attractive method for producing the next generation of carbon composite materials with a high power performance in supercapacitors working in neutral medium. PMID:23794416

  18. Photocatalytic Oxidation of Volatile Organic Compounds Over Electrospun Activated TIO2/CARBON Nanofiber Composite

    NASA Astrophysics Data System (ADS)

    Gholamvand, Zahra; Aboutalebi, Seyed Hamed; Keyanpour-Rad, Mansoor

    In this study, TiO2/PAN-based fibers were prepared by electrospinning a composite solution containing both the desirable contents of TiO2 and a 10 wt. % PAN polymer solution dissolved in N, N-dimethylformamide. The TiO2 loaded electrospun PAN nanofibers were then carbonized at 1000 °C in N2 atmosphere furnace after stabilization at 230 °C in air. Then CNF/TiO2 nanofibers were oxidized at 450 °C in air. The morphology and structure of the TiO2-embeded carbon nanofibers were investigated by SEM and Raman spectroscopy. Specific surface area was determined using BET equation from N2 adsorption analysis. Photocatalytic tests were conducted in a UV illuminated set-up specialized for the filters using ethanol vapor. The results have shown that ethanol vapor was efficiently degraded on TiO2/CNF composite nanofiber mat under UV illumination. The aim of this study was to further investigate the feasibility of TiO2/ACF for practical indoor air purification.

  19. Protection of porous carbon fuel particles from boudouard corrosion

    SciTech Connect

    Cooper, John F.

    2015-05-26

    A system for producing energy that includes infusing porous carbon particles produced by pyrolysis of carbon-containing materials with an off-eutectic salt composition thus producing pore-free carbon particles, and reacting the carbon particles with oxygen in a fuel cell according to the reaction C+O.sub.2=CO.sub.2 to produce electrical energy.

  20. High photocatalytic activity of V-doped SrTiO3 porous nanofibers produced from a combined electrospinning and thermal diffusion process

    PubMed Central

    Jing, Panpan; Su, Qing; Xie, Erqing

    2015-01-01

    Summary In this letter, we report a novel V-doped SrTiO3 photocatalyst synthesized via electrospinning followed by a thermal diffusion process at low temperature. The morphological and crystalline structural investigations reveal not only that the V-doped SrTiO3 photocatalyst possesses a uniform, porous, fibrous structure, but also that some V5+ ions are introduced into the SrTiO3 lattice. The photocatalytic capability of V-doped SrTiO3 porous nanofibers was evaluated through photodegrading methyl orange (MO) in aqueous solution under artificial UV–vis light. The results indicated that V-doped SrTiO3 porous nanofibers have excellent catalytic efficiency. Furthermore, the excellent catalytic activity was maintained even after five cycle tests, indicating that they have outstanding photocatalytic endurance. It is suggested that the excellent photocatalytic performance of doped SrTiO3 nanofibers is possibly attributed to the V5+ ion doping increasing the light utilization as well as to the outstanding porous features, the excellent component and structure stability. PMID:26199831

  1. Laccase Biosensor Based on Electrospun Copper/Carbon Composite Nanofibers for Catechol Detection

    PubMed Central

    Fu, Jiapeng; Qiao, Hui; Li, Dawei; Luo, Lei; Chen, Ke; Wei, Qufu

    2014-01-01

    The study compared the biosensing properties of laccase biosensors based on carbon nanofibers (CNFs) and copper/carbon composite nanofibers (Cu/CNFs). The two kinds of nanofibers were prepared by electrospinning and carbonization under the same conditions. Scanning electron microscopy (SEM), X-ray diffraction (XRD) and Raman spectroscopy were employed to investigate the morphologies and structures of CNFs and Cu/CNFs. The amperometric results indicated that the Cu/CNFs/laccase(Lac)/Nafion/glass carbon electrode (GCE) possessed reliable analytical performance for the detection of catechol. The sensitivity of the Cu/CNFs/Lac/Nafion/GCE reached 33.1 μA/mM, larger than that of CNFs/Lac/Nafion/GCE. Meanwhile, Cu/CNFs/Lac/Nafion/GCE had a wider linear range from 9.95 × 10−6 to 9.76 × 10−3 M and a lower detection limit of 1.18 μM than CNFs/Lac/Nafion/GCE. Moreover, it exhibited a good repeatability, reproducibility, selectivity and long-term stability, revealing that electrospun Cu/CNFs have great potential in biosensing. PMID:24561403

  2. Anchoring Fe3O4 nanoparticles on three-dimensional carbon nanofibers toward flexible high-performance anodes for lithium-ion batteries

    NASA Astrophysics Data System (ADS)

    Wan, Yizao; Yang, Zhiwei; Xiong, Guangyao; Guo, Ruisong; Liu, Ze; Luo, Honglin

    2015-10-01

    There is growing interest in flexible, cost-effective, and binder-free energy storage devices to meet the special needs of modern electronic systems. Herein we report a general, scalable, eco-friendly, and cost-effective approach for the fabrication of nano-Fe3O4-anchored three-dimensional (3D) carbon nanofiber (CNFs) aerogels (Fe3O4@BC-CNFs). The preparation processes include the anchoring of Fe2O3 nanoparticles on bacterial cellulose (BC) nanofibers with intrinsic 3D network structure and subsequent carbonization at different temperatures. The aerogel carbonized at 600 °C (Fe3O4@BC-CNFs-600) is highly flexible and was directly used as working electrodes in lithium-ion batteries without metal current collectors, conducting additives, or binders. The Fe3O4@BC-CNFs-600 demonstrates greatly improved electrochemical performance in comparison to the bare Fe3O4 nanoparticles. In addition to its excellent flexibility, a stable capacity of 755 mAh g-1 for up to 80 cycles is also higher than most of carbon-Fe3O4 hybrids. The high reversible capacity and excellent rate capability are attributed to its 3D porous network structure with well-dispersed Fe3O4 nanoparticles on the surfaces of CNFs.

  3. Preparation of flexible zinc oxide/carbon nanofiber webs for mid-temperature desulfurization

    NASA Astrophysics Data System (ADS)

    Kim, Soojung; Bajaj, Bharat; Byun, Chang Ki; Kwon, Soon-Jin; Joh, Han-Ik; Yi, Kwang Bok; Lee, Sungho

    2014-11-01

    Polyacrylonitrile (PAN) derived carbon nanofiber (CNF) webs loaded with zinc oxide (ZnO) were synthesized using electrospinning and heat treatment at 600 °C. Uniformly dispersed ZnO nanoparticles, clarified by X-ray diffraction and scanning electron microscopy, were observed on the surface of the nanofiber composites containing 13.6-29.5 wt% of ZnO. The further addition of ZnO up to 34.2 wt% caused agglomeration with a size of 50-80 nm. Higher ZnO contents led the concentrated ZnO nanoparticles on the surface of the nanofibers rather than uniform dispersion along the cross-section of the fiber. The flexible composite webs were crushed and tested for hydrogen sulfide (H2S) adsorption at 300 °C. Breakthrough experiments with the ZnO/CNF composite containing 25.7 wt% of ZnO for H2S adsorption showed three times higher ZnO utilization efficiency compared to pure ZnO nano powders, attributed to chemisorption of the larger surface area of well dispersed ZnO particles on nanofibers and physical adsorption of CNF.

  4. Electrospun polyvinyl alcohol/carbon dioxide modified polyethyleneimine composite nanofiber scaffolds.

    PubMed

    Wu, Han-Bing; Bremner, David H; Nie, Hua-Li; Quan, Jing; Zhu, Li-Min

    2015-05-01

    A novel biocompatible polyvinyl alcohol/carbon dioxide modified polyethyleneimine (PVA/PEI-CO2) composite nanofiber was fabricated by a green and facile protocol, which reduces the cytotoxicity of PEI through the surface modification of the PEI with CO2. The (13)C NMR spectrum, elemental analysis, and TGA show that CO2 has been incorporated in the PEI surface resulting in a relatively stable structure. The resulting PVA/PEI-CO2 composite nanofibers have been characterized by attenuated total reflection-Fourier transform infrared spectroscopy (ATR-FTIR), contact angle, and scanning electron microscopy (SEM). The results show that the average diameters of the nanofibers range from 265 ± 53 nm to 423 ± 80 nm. The cytotoxicity of PVA/PEI-CO2 composite nanofibers was assessed by cytotoxicity evaluation using the growth and cell proliferation of normal mice Schwann cells. SEM and the MTT assay demonstrated the promotion of cell growth and proliferation on the PVA/PEI-CO2 composite scaffold. It suggests that PEI-CO2 can have tremendous potential applications in biological material research. PMID:25540321

  5. Self-floating graphitic carbon nitride/zinc phthalocyanine nanofibers for photocatalytic degradation of contaminants.

    PubMed

    Xu, Tiefeng; Ni, Dongjing; Chen, Xia; Wu, Fei; Ge, Pengfei; Lu, Wangyang; Hu, Hongguang; Zhu, ZheXin; Chen, Wenxing

    2016-11-01

    The effective elimination of micropollutants by an environmentally friendly method has received extensive attention recently. In this study, a photocatalyst based on polyacrylonitrile (PAN)-supported graphitic carbon nitride coupled with zinc phthalocyanine nanofibers (g-C3N4/ZnTcPc/PAN nanofibers) was successfully prepared, where g-C3N4/ZnTcPc was introduced as the catalytic entity and the PAN nanofibers were employed as support to overcome the defects of easy aggregation and difficult recycling. Herein, rhodamine B (RhB), 4-chlorophenol and carbamazepine (CBZ) were selected as the model pollutants. Compared with the typical hydroxyl radical-dominated catalytic system, g-C3N4/ZnTcPc/PAN nanofibers displayed the targeted adsorption and degradation of contaminants under visible light or solar irradiation in the presence of high additive concentrations. According to the results of the radical scavenging techniques and the electron paramagnetic resonance technology, the degradation of target substrates was achieved by the attack of active species, including photogenerated hole, singlet oxygen, superoxide radicals and hydroxyl radicals. Based on the results of ultra-performance liquid chromatography and mass spectrometry, the role of free radicals on the photocatalytic degradation intermediates was identified and the final photocatalytic degradation products of both RhB and CBZ were some biodegradable small molecules. PMID:27239724

  6. Vertically aligned carbon nanofiber as nano-neuron interface for monitoring neural function

    SciTech Connect

    Ericson, Milton Nance; McKnight, Timothy E; Melechko, Anatoli Vasilievich; Simpson, Michael L; Morrison, Barclay; Yu, Zhe

    2012-01-01

    Neural chips, which are capable of simultaneous, multi-site neural recording and stimulation, have been used to detect and modulate neural activity for almost 30 years. As a neural interface, neural chips provide dynamic functional information for neural decoding and neural control. By improving sensitivity and spatial resolution, nano-scale electrodes may revolutionize neural detection and modulation at cellular and molecular levels as nano-neuron interfaces. We developed a carbon-nanofiber neural chip with lithographically defined arrays of vertically aligned carbon nanofiber electrodes and demonstrated its capability of both stimulating and monitoring electrophysiological signals from brain tissues in vitro and monitoring dynamic information of neuroplasticity. This novel nano-neuron interface can potentially serve as a precise, informative, biocompatible, and dual-mode neural interface for monitoring of both neuroelectrical and neurochemical activity at the single cell level and even inside the cell.

  7. Preparation and Study on Nickel Oxide Reduction of Polyacrylonitrile-Based Carbon Nanofibers by Thermal Treatment.

    PubMed

    Lee, Yeong Ju; Kim, Hyun Bin; Jeun, Joon Pyo; Lee, Dae Soo; Koo, Dong Hyun; Kang, Phil Hyun

    2015-08-01

    Carbon materials containing magnetic nanopowder have been attractive in technological applications such as electrochemical capacitors and electromagnetic wave shielding. In this study, polyacrylonitrile (PAN) fibers containing nickel nanoparticles were prepared using an electrospinning method and thermal stabilization. The reduction of nickel oxide was investigated under a nitrogen atmosphere within a temperature range of 600 to 1,000 °C. Carbon nanofibers containing nickel nanoparticles were characterized by FE-SEM, EDS, XRD, TGA, and VSM. It was found that nickel nanoparticles were formed by a NiO reduction in PAN as a function of the thermal treatment. These results led to an increase in the coercivity of nanofibers and a decrease in the remanence magnetization. PMID:26369192

  8. Effects of vapor grown carbon nanofibers on electrical and mechanical properties of a thermoplastic elastomer

    NASA Astrophysics Data System (ADS)

    Basaldua, Daniel Thomas

    Carbon nanofiber (CNF) reinforced composites are exceptional materials that exhibit superior properties compared to conventional composites. This paper presents the development of a vapor grown carbon nanofiber (VGCNF) thermoplastic polyurethane (TPU) composite by a melt mixing process. Dispersion and distribution of CNFs inside the TPU matrix were examined through scanning electron microscopy to determine homogeneity. The composite material underwent durometer, thermal gravimetric analysis, differential scanning calorimetry, heat transfer, hysteresis, dynamic modulus, creep, tensile, abrasion, and electrical conductivity testing to characterize its properties and predict behavior. The motivation for this research is to develop an elastomer pad that is an electrically conductive alternative to the elastomer pads currently used in railroad service. The material had to be a completely homogenous electrically conductive CNF composite that could withstand a harsh dynamically loaded environment. The new material meets mechanical and conductive requirements for use as an elastomer pad in a rail suspension.

  9. Controllable synthesis of helical, straight, hollow and nitrogen-doped carbon nanofibers and their magnetic properties

    SciTech Connect

    Li, Xun; Xu, Zheng

    2012-12-15

    Graphical abstract: The helical, straight and hollow carbon nanofibers can be selectively synthesized by adjusting either the reaction temperature or feed gas composition. Display Omitted Highlights: ► CNFs were synthesized via pyrolysis of acetylene on copper NPs. ► The helical, straight, hollow and N-doped CNFs can be selectively synthesized. ► The growth mechanism of different types of CNFs was proposed. -- Abstract: Carbon nanofibers (CNFs) with various morphologies were synthesized by catalytic pyrolysis of acetylene on copper nanoparticles which were generated from the in situ decomposition of copper acetylacetonate. The morphology of the pristine and acid-washed CNFs was investigated by field emission scanning electron microscope and high-resolution transmission electron microscope. Helical, straight and hollow CNFs can be selectively synthesized by adjusting either the reaction temperature or feed gas composition. The growth mechanism for these three types of CNFs was proposed.

  10. High-strength porous carbon and its multifunctional applications

    SciTech Connect

    Wojtowicz, Marek A; Rubenstein, Eric P; Serio, Michael A; Cosgrove, Joseph E

    2013-12-31

    High-strength porous carbon and a method of its manufacture are described for multifunctional applications, such as ballistic protection, structural components, ultracapacitor electrodes, gas storage, and radiation shielding. The carbon is produced from a polymer precursor via carbonization, and optionally by surface activation and post-treatment.

  11. Label-Free Detection of Cardiac Troponin-I Using Carbon Nanofiber Based Nanoelectrode Arrays

    NASA Technical Reports Server (NTRS)

    Periyakaruppan, Adaikkappan; Koehne, Jessica Erin; Gandhiraman, Ram P.; Meyyappan, M.

    2013-01-01

    A sensor platform based on vertically aligned carbon nanofibers (CNFs) has been developed. Their inherent nanometer scale, high conductivity, wide potential window, good biocompatibility and well-defined surface chemistry make them ideal candidates as biosensor electrodes. A carbon nanofiber (CNF) multiplexed array has been fabricated with 9 sensing pads, each containing 40,000 carbon nanofibers as nanoelectrodes. Here, we report the use of vertically aligned CNF nanoelectrodes for the detection of cardiac Troponin-I for the early diagnosis of myocardial infarction. Antibody, antitroponin, probe immobilization and subsequent binding to human cardiac troponin-I were characterized using electrochemical impedance spectroscopy and cyclic voltammetry techniques. Each step of the modification process resulted in changes in electrical capacitance or resistance to charge transfer due to the changes at the electrode surface upon antibody immobilization and binding to the specific antigen. This sensor demonstrates high sensitivity, down to 0.2 ng/mL, and good selectivity making this platform a good candidate for early stage diagnosis of myocardial infarction.

  12. Electrochemical properties of oxygenated cup-stacked carbon nanofiber-modified electrodes.

    PubMed

    Ko, Seongjae; Tatsuma, Tetsu; Sakoda, Akiyoshi; Sakai, Yasuyuki; Komori, Kikuo

    2014-06-28

    Oxygenated cup-stacked carbon nanofibers (CSCNFs), the surface of which provides highly ordered graphene edges and oxygen-containing functional groups, were investigated as electrode materials by using typical redox species in electrochemistry, Fe(2+/3+), [Fe(CN)6](3-/4-), and dopamine. The electron transfer rates for these redox species at oxygenated CSCNF electrodes were higher than those at edge-oriented pyrolytic graphite and glassy carbon electrodes. In addition, the oxygen-containing functional groups also contributed to the electron transfer kinetics at the oxygenated CSCNF surface. The electron transfer rate of Fe(2+/3+) was accelerated and that of [Fe(CN)6](3-/4-) was decelerated by the oxygen-containing groups, mainly due to the electrostatic attraction and repulsion, respectively. The electrochemical reaction selectivities at the oxygenated CSCNF surface were tunable by controlling the amount of nanofibers and the oxygen/carbon atomic ratio at the nanofiber surface. Thus, the oxygenated CSCNFs would be useful electrode materials for energy-conversion, biosensing, and other electrochemical devices. PMID:24817367

  13. Growth of carbon nanofibers on carbon fabric with Ni nanocatalyst prepared using pulse electrodeposition

    NASA Astrophysics Data System (ADS)

    Hung, Kai-Hsuan; Tzeng, Shinn-Shyong; Kuo, Wen-Shyong; Wei, Bingqing; Ko, Tse-Hao

    2008-07-01

    The pulse electrodeposition (PED) technique was utilized to deposit nanosized (<=10 nm) Ni catalysts on carbon fabric (CF). Via an in situ potential profile, the PED technique can control the Ni catalyst loading, which is an important parameter for the growth of carbon nanofibers (CNFs) on CF. The preparation of CNF-coated CF (carpet-like CF) was carried out in a thermal chemical vapor deposition system with an optimum loading of Ni catalysts deposited in the PED pulse range from 20 to 320 cycles. CNFs grown at 813 K using different pulse cycles had a narrow diameter distribution, around 15 ± 5 nm to 29 ± 7 nm they have a hydrophobic surface, like lotus leaves. Transmission electron microscopy images confirmed the graphene structural transformation of CNFs with the growth temperature. Solid wire CNFs were initially grown at 813 K with graphene edges exposed on the external surface. At elevated growth temperatures (1073 and 1173 K), bamboo-like CNFs were obtained, with herringbone structures and intersectional hollow cores.

  14. Chemical vapor-deposited carbon nanofibers on carbon fabric for supercapacitor electrode applications

    PubMed Central

    2012-01-01

    Entangled carbon nanofibers (CNFs) were synthesized on a flexible carbon fabric (CF) via water-assisted chemical vapor deposition at 800°C at atmospheric pressure utilizing iron (Fe) nanoparticles as catalysts, ethylene (C2H4) as the precursor gas, and argon (Ar) and hydrogen (H2) as the carrier gases. Scanning electron microscopy, transmission electron microscopy, and electron dispersive spectroscopy were employed to characterize the morphology and structure of the CNFs. It has been found that the catalyst (Fe) thickness affected the morphology of the CNFs on the CF, resulting in different capacitive behaviors of the CNF/CF electrodes. Two different Fe thicknesses (5 and 10 nm) were studied. The capacitance behaviors of the CNF/CF electrodes were evaluated by cyclic voltammetry measurements. The highest specific capacitance, approximately 140 F g−1, has been obtained in the electrode grown with the 5-nm thickness of Fe. Samples with both Fe thicknesses showed good cycling performance over 2,000 cycles. PMID:23181897

  15. Antitumor Activity of Doxorubicin-Loaded Carbon Nanotubes Incorporated Poly(Lactic-Co-Glycolic Acid) Electrospun Composite Nanofibers

    NASA Astrophysics Data System (ADS)

    Yu, Yuan; Kong, Lijun; Li, Lan; Li, Naie; Yan, Peng

    2015-08-01

    The drug-loaded composite electrospun nanofiber has attracted more attention in biomedical field, especially in cancer therapy. In this study, a composite nanofiber was fabricated by electrospinning for cancer treatment. Firstly, the carbon nanotubes (CNTs) were selected as carriers to load the anticancer drug—doxorubicin (DOX) hydrochloride. Secondly, the DOX-loaded CNTs (DOX@CNTs) were incorporated into the poly(lactic-co-glycolic acid) (PLGA) nanofibers via electrospinning. Finally, a new drug-loaded nanofibrous scaffold (PLGA/DOX@CNTs) was formed. The properties of the prepared composite nanofibrous mats were characterized by various techniques. The release profiles of the different DOX-loaded nanofibers were measured, and the in vitro antitumor efficacy against HeLa cells was also evaluated. The results showed that DOX-loaded CNTs can be readily incorporated into the nanofibers with relatively uniform distribution within the nanofibers. More importantly, the drug from the composite nanofibers can be released in a sustained and prolonged manner, and thereby, a significant antitumor efficacy in vitro is obtained. Thus, the prepared composite nanofibrous mats are a promising alternative for cancer treatment.

  16. Preparation and electrochemical properties of carbon-coated LiFePO4 hollow nanofibers

    NASA Astrophysics Data System (ADS)

    Wei, Bin-bin; Wu, Yan-bo; Yu, Fang-yuan; Zhou, Ya-nan

    2016-04-01

    Carbon-coated LiFePO4 hollow nanofibers as cathode materials for Li-ion batteries were obtained by coaxial electrospinning. X-ray diffraction, scanning electron microscopy, transmission electron microscopy, Brunauer-Emmett-Teller specific surface area analysis, galvanostatic charge-discharge, and electrochemical impedance spectroscopy (EIS) were employed to investigate the crystalline structure, morphology, and electrochemical performance of the as-prepared hollow nanofibers. The results indicate that the carbon-coated LiFePO4 hollow nanofibers have good long-term cycling performance and good rate capability: at a current density of 0.2C (1.0C = 170 mA·g-1) in the voltage range of 2.5-4.2 V, the cathode materials achieve an initial discharge specific capacity of 153.16 mAh·g-1 with a first charge-discharge coulombic efficiency of more than 97%, as well as a high capacity retention of 99% after 10 cycles; moreover, the materials can retain a specific capacity of 135.68 mAh·g-1, even at 2C.

  17. Exposure and Emissions Monitoring during Carbon Nanofiber Production—Part II: Polycyclic Aromatic Hydrocarbons

    PubMed Central

    BIRCH, M. EILEEN

    2015-01-01

    Production of carbon nanofibers and nanotubes (CNFs/CNTs) and their composite products is increasing globally. High-volume production may increase the exposure risks for workers who handle these materials. Though health effects data for CNFs/CNTs are limited, some studies raise serious health concerns. Given the uncertainty about their potential hazards, there is an immediate need for toxicity data and field studies to assess exposure to CNFs/CNTs. An extensive study was conducted at a facility that manufactures and processes CNFs. Filter, sorbent, cascade impactor, bulk, and microscopy samples, combined with direct-reading instruments, provided complementary information on air contaminants. Samples were analyzed for organic and elemental carbon (OC and EC), metals, and polycyclic aromatic hydrocarbons (PAHs), with EC as a measure of CNFs. Transmission electron microscopy with energy-dispersive X-ray spectroscopy also was applied. Fine/ultrafine iron-rich soot, PAHs, and carbon monoxide were production byproducts. Direct-reading instrument results were reported previously [Evans DE et al. (Aerosol monitoring during carbon nanofiber production: mobile direct-reading sampling. Ann Occup Hyg 2010; 54:514–31)]. Results for time-integrated samples are reported as companion papers in this issue. OC and EC, metals, and microscopy results are reported in Part I [Birch ME et al. (Exposure and emissions monitoring during carbon nanofiber production—Part I: elemental carbon and iron–soot aerosols. Ann Occup Hyg 2011; 55: 1016–36.)] whereas results for PAHs are reported here. Naphthalene and acenaphthylene were the dominant PAHs with average concentrations ranging from 115 to 336 μg m−3 and 35 to 84 μg m−3, respectively. Concentrations of other PAHs ranged from ~1 to 10 μg m−3. PMID:21976308

  18. Preparation and characterization of Polyacrylonitrile/ Manganese Dioxides- based Carbon Nanofibers via electrospinning process

    NASA Astrophysics Data System (ADS)

    Che Othman, F. E.; Yusof, N.; Jaafar, J.; Ismail, A. F.; Hasbullah, H.; Abdullah, N.; Ismail, M. S.

    2016-06-01

    This research reports the production of precursor polyacrylonitrile (PAN)/ manganese dioxide (MnO2) nanofibers (NFs) via electrospinning method followed by stabilization and carbonization processes. Nowadays, electrospinning has become a suitable method in manufacturing continuous NFs, thus it is employed to fabricate NFs in this study. The microstructural properties and adsorption competencies of the produced NFs were also studied. The NFs were prepared by electrospinning the polymer solution of Polyacrylonitrile (PAN) and Manganese Dioxide (MnO2) in, N, N-Dimethylformamide (DMF) solvent. The factors considered in this study were various polymer PAN/MnO2 concentrations which will significantly affect the specific surface area, fiber morphology and the diameter of the NFs prepared. Subsequently, heat treatment is applied by setting up the stabilization temperature at 275 °C and carbonization temperature at 800 °C with constant dwelling time (30 min). Nitrogen gas at constant rate 0.2 L/min was used for stabilization and carbonization with the stabilization rate (2 °C/min) and carbonization rate (5 °C/min). The carbon nanofibers (CNFs) produced were characterized using Scanning Electron Microscopy (SEM), Brunauer Emmett and Teller (BET) surface area and Fourier Transmission Infrared Spectroscopy (FTIR). It was found that the PAN/MnO2 CNFs were successfully produced with the carbonization temperature of 800 °C. The prepared PAN/MnO2 CNFs prepared showed an enhanced in specific surface area about two times compared to it precursor NFs.

  19. Characterization of carbon nanofiber mats produced from electrospun lignin-g-polyacrylonitrile copolymer.

    PubMed

    Youe, Won-Jae; Lee, Soo-Min; Lee, Sung-Suk; Lee, Seung-Hwan; Kim, Yong Sik

    2016-01-01

    The graft copolymerization of acrylonitrile (AN) onto methanol-soluble kraft lignin (ML) was achieved through a two-step process in which AN was first polymerized with an α,α'-azobisisobutyronitrile initiator, followed by radical coupling with activated ML. A carbon nanofiber material was obtained by electrospinning a solution of this copolymer in N,N-dimethylformamide, then subjecting it to a heat treatment including thermostabilization at 250°C and subsequent carbonization at 600-1400°C. Increasing the carbonization temperature was found to increase the carbon content of the resulting carbon nanofibers from 70.5 to 97.1%, which had the effect of increasing their tensile strength from 35.2 to 89.4 MPa, their crystallite size from 13.2 to 19.1 nm, and their electrical conductivity from ∼0 to 21.3 Scm(-1). The morphology of the mats, in terms of whether they experienced beading or not, was found to be dependent on the concentration of the initial electrospinning solution. From these results, it is proposed that these mats could provide the basis for a new class of carbon fiber material. PMID:26459170

  20. Iron Carbide Nanoparticles Encapsulated in Mesoporous Fe-N-Doped Carbon Nanofibers for Efficient Electrocatalysis.

    PubMed

    Wu, Zhen-Yu; Xu, Xing-Xing; Hu, Bi-Cheng; Liang, Hai-Wei; Lin, Yue; Chen, Li-Feng; Yu, Shu-Hong

    2015-07-01

    Exploring low-cost and high-performance nonprecious metal catalysts (NPMCs) for oxygen reduction reaction (ORR) in fuel cells and metal-air batteries is crucial for the commercialization of these energy conversion and storage devices. Here we report a novel NPMC consisting of Fe3 C nanoparticles encapsulated in mesoporous Fe-N-doped carbon nanofibers, which is synthesized by a cost-effective method using carbonaceous nanofibers, pyrrole, and FeCl3 as precursors. The electrocatalyst exhibits outstanding ORR activity (onset potential of -0.02 V and half-wave potential of -0.140 V) closely comparable to the state-of-the-art Pt/C catalyst in alkaline media, and good ORR activity in acidic media, which is among the highest reported activities of NPMCs. PMID:26014581

  1. Aerosynthesis: Growths of Vertically Aligned Carbon Nanofibers with Air DC Plasma

    SciTech Connect

    Kodumagulla, A; Varanasi, V; Pearce, Ryan; Wu, W-C; Hensley, Dale K; Tracy, Joseph B; McKnight, Timothy E; Melechko, Anatoli

    2014-01-01

    Vertically aligned carbon nanofibers (VACNF) have been synthesized in a mixture of acetone and air using catalytic DC plasma enhanced chemical vapor deposition. Typically, ammonia or hydrogen is used as etchant gas in the mixture to remove carbon that otherwise passivates the catalyst surface and impedes growth. Our demonstration of using air as the etchant gas opens up a possibility that ion etching could be sufficient to maintain the catalytic activity state during synthesis. It also demonstrates the path toward growing VACNFs in open atmosphere.

  2. Reinforcement and rupture behavior of carbon nanotubes-polymer nanofibers

    NASA Astrophysics Data System (ADS)

    Ye, Haihui; Lam, Hoa; Titchenal, Nick; Gogotsi, Yury; Ko, Frank

    2004-09-01

    High-resolution transmission electron microscopy examination of carbon nanotube-polyacrylonitrile composite fibers synthesized by electrospinning was conducted. Both single-wall carbon nanotubes and multi-wall carbon nanotubes have been used to reinforce the polymer fibers. A two-stage rupture behavior of the composite fibers under tension, including crazing of polymer matrix and pull-out of carbon nanotubes, has been observed. Carbon nanotubes reinforce the polymer fibers by hindering crazing extension, reducing stress concentration, and dissipating energy by pullout. Distribution of nanotubes in the polymer matrix and interfacial adhesion between nanotubes and polymers are two major factors to determine the reinforcement effect of carbon nanotubes in polymer fibers.

  3. Influence of the support on the structural characteristics of carbon nanofibers produced from the metal-catalyzed decomposition of ethylene

    SciTech Connect

    Anderson, P.E.; Rodriguez, N.M.

    2000-03-01

    The notion of using support materials to achieve high dispersions of metal particles has been extended to the synthesis of carbon nanofibers from the catalyzed decomposition of ethylene. By using this approach it has been possible to generate nanofibers whose widths are dictated by the dimensions of the supported metal particles. In addition, the support may alter the state of the bulk and/or the surface of the catalyst particle through metal-support interactions, and the impact of this effect is manifested by modifications in the structural characteristics of the nanofibers deposits. In an attempt to gain a clearer insight into the influence of metal-support interaction on the growth characteristics of GNF, three metals, FE,Ni, and Co that are known to be active catalysts for this process were impregnated onto silica, graphite, and well-characterized graphite nanofiber supports. Characterization of the solid carbon products was performed by a variety of approaches including high-resolution transmission electron microscopy (HRTEM), gas-phase analysis, and thermal-programmed oxidation (TPO). The goal of this study was to correlate each nanofiber product with the behavior of the specific metal/support precursor system. The advantages of using selected support materials to control the morphologies and sizes of nanofibers is present.

  4. Method for the preparation of ferrous low carbon porous material

    DOEpatents

    Miller, Curtis Jack

    2014-05-27

    A method for preparing a porous metal article using a powder metallurgy forming process is provided which eliminates the conventional steps associated with removing residual carbon. The method uses a feedstock that includes a ferrous metal powder and a polycarbonate binder. The polycarbonate binder can be removed by thermal decomposition after the metal article is formed without leaving a carbon residue.

  5. Mass-transport-controlled, large-area, uniform deposition of carbon nanofibers and their application in gas diffusion layers of fuel cells.

    PubMed

    Tang, Xian; Xie, Zhiyong; Huang, Qizhong; Chen, Guofen; Hou, Ming; Yi, Baolian

    2015-05-01

    The effect of mass transport on the growth characteristics of large-area vapor-grown carbon nanofibers (CNFs) was investigated by adjusting the substrate deposition angle (α). The catalyst precursor solution was coated onto one side of a 2D porous carbon paper substrate via a decal printing method. The results showed that the CNFs were grown on only one side of the substrate and α was found to significantly affect the growth uniformity. At α = 0°, the growth thickness, the density, the microstructure and the yield of the CNF film were uniform across the substrate surface, whereas the growth uniformity decreased with increasing α, suggesting that the large-area CNF deposition processes were mass-transport-controlled. Computational fluid dynamics simulations of the gas diffusion processes revealed the homogeneous distributions of the carbon-source-gas concentration, pressure, and velocity near the substrate surface at α = 0°, which were the important factors in achieving the mass-transport-limited uniform CNF growth. The homogeneity of the field distributions decreased with increasing α, in accordance with the variation in the growth uniformity with α. When used as a micro-porous layer, the uniform CNF film enabled higher proton exchange membrane fuel cell performance in comparison with commercial carbon black by virtue of its improved electronic and mass-transport properties confirmed by the electrochemical impedance spectroscopy results. PMID:25865711

  6. A general approach to fabricate free-standing metal sulfide@carbon nanofiber networks as lithium ion battery anodes.

    PubMed

    Fei, Ling; Williams, Brian Patrick; Yoo, Sang Ha; Carlin, Joseph Michael; Joo, Yong Lak

    2016-01-25

    A general approach for fabricating free-standing metal sulfide and carbon nanofiber mats is developed via electrospinning, starting with cheap and abundant raw materials. The prepared free-standing samples have metal sulfide nanoparticles dispersed throughout the interconnected carbon fibers. When applied to LIB, the composites demonstrate excellent cyclability and rate capability. PMID:26659850

  7. Elastic and hierarchical porous carbon nanofibrous membranes incorporated with NiFe2O4 nanocrystals for highly efficient capacitive energy storage

    NASA Astrophysics Data System (ADS)

    Ge, Jianlong; Fan, Gang; Si, Yang; He, Jianxin; Kim, Hak-Yong; Ding, Bin; Al-Deyab, Salem S.; El-Newehy, Mohamed; Yu, Jianyong

    2016-01-01

    Flexible membranes created from porous carbon nanofibers (CNFs) hold great promise in the next generation wearable energy storage devices, but challenges still remain due to the poor mechanical properties of porous carbon nanofibers. Here, we report a facile strategy to fabricate elastic and hierarchical porous CNF membranes with NiFe2O4 nanocrystals embedded via multicomponent electrospinning and nano-doping methods. Benefiting from the scattering effect of NiFe2O4 nanocrystals and graphitized carbon layers for the condensed stress, the resultant CNF membranes exhibit an enhanced elasticity with a bending radius <12 μm, rapid recovery from the deformations, and a superior softness. Quantitative pore size distribution and fractal analysis reveal that the CNFs possessed tunable porous structures with a high surface area of 493 m2 g-1 and a pore volume of 0.31 cm3 g-1. Benefiting from the robust mechanical stability, hierarchical porous structures and good electrochemical properties, the NiFe2O4 doped CNF membranes demonstrate a high electrical capacitance of 343 F g-1, and good reversibility with a cycling efficiency of 97.4% even after 10 000 cycles. The successful synthesis of elastic porous CNF membranes also provided a versatile platform for the design and development of functional CNF based materials for various applications.Flexible membranes created from porous carbon nanofibers (CNFs) hold great promise in the next generation wearable energy storage devices, but challenges still remain due to the poor mechanical properties of porous carbon nanofibers. Here, we report a facile strategy to fabricate elastic and hierarchical porous CNF membranes with NiFe2O4 nanocrystals embedded via multicomponent electrospinning and nano-doping methods. Benefiting from the scattering effect of NiFe2O4 nanocrystals and graphitized carbon layers for the condensed stress, the resultant CNF membranes exhibit an enhanced elasticity with a bending radius <12 μm, rapid recovery

  8. Control of physical properties of carbon nanofibers obtained from coaxial electrospinning of PMMA and PAN with adjustable inner/outer nozzle-ends.

    PubMed

    Kaerkitcha, Navaporn; Chuangchote, Surawut; Sagawa, Takashi

    2016-12-01

    Hollow carbon nanofibers (HCNFs) were prepared by electrospinning method with several coaxial nozzles, in which the level of the inner nozzle-end is adjustable. Core/shell nanofibers were prepared from poly(methyl methacrylate) (PMMA) as a pyrolytic core and polyacrylonitrile (PAN) as a carbon shell with three types of normal (viz. inner and outer nozzle-ends are balanced in the same level), inward, and outward coaxial nozzles. The influence of the applied voltage on these three types of coaxial nozzles was studied. Specific surface area, pore size diameter, crystallinity, and degree of graphitization of the hollow and mesoporous structures of carbon nanofibers obtained after carbonization of the as spun PMMA/PAN nanofibers were characterized by BET analyses, X-ray diffraction, and Raman spectroscopy in addition to the conductivity measurements. It was found that specific surface area, crystallinity, and graphitization degree of the HCNFs affect the electrical conductivity of the carbon nanofibers. PMID:27067734

  9. Control of physical properties of carbon nanofibers obtained from coaxial electrospinning of PMMA and PAN with adjustable inner/outer nozzle-ends

    NASA Astrophysics Data System (ADS)

    Kaerkitcha, Navaporn; Chuangchote, Surawut; Sagawa, Takashi

    2016-04-01

    Hollow carbon nanofibers (HCNFs) were prepared by electrospinning method with several coaxial nozzles, in which the level of the inner nozzle-end is adjustable. Core/shell nanofibers were prepared from poly(methyl methacrylate) (PMMA) as a pyrolytic core and polyacrylonitrile (PAN) as a carbon shell with three types of normal (viz . inner and outer nozzle-ends are balanced in the same level), inward, and outward coaxial nozzles. The influence of the applied voltage on these three types of coaxial nozzles was studied. Specific surface area, pore size diameter, crystallinity, and degree of graphitization of the hollow and mesoporous structures of carbon nanofibers obtained after carbonization of the as spun PMMA/PAN nanofibers were characterized by BET analyses, X-ray diffraction, and Raman spectroscopy in addition to the conductivity measurements. It was found that specific surface area, crystallinity, and graphitization degree of the HCNFs affect the electrical conductivity of the carbon nanofibers.

  10. Carbon nanotube-templated polyaniline nanofibers: synthesis, flash welding and ultrafiltration membranes.

    PubMed

    Liao, Yaozu; Yu, Deng-Guang; Wang, Xia; Chain, Wei; Li, Xin-Gui; Hoek, Eric M V; Kaner, Richard B

    2013-05-01

    Electro-active switchable ultrafiltration membranes are of great interest due to the possibility of external control over permeability, selectivity, anti-fouling and cleaning. Here, we report on hybrid single-walled carbon nanotube (SWCNT)-polyaniline (PANi) nanofibers synthesized by in situ polymerization of aniline in the presence of oxidized SWCNTs. The composite nanofibers exhibit unique morphology of core-shell (SWCNT-PANi) structures with average total diameters of 60 nm with 10 to 30 nm thick PANi coatings. The composite nanofibers are easily dispersed in polar aprotic solvents and cast into asymmetric membranes via a nonsolvent induced phase separation. The hybrid SWCNT-PANi membranes are electrically conductive at neutral pH and exhibit ultrafiltration-like permeability and selectivity when filtering aqueous suspensions of 6 nm diameter bovine serum albumin and 48 nm diameter silica particles. A novel flash welding technique is utilized to tune the morphology, porosity, conductivity, permeability and nanoparticle rejection of the SWCNT-PANi composite ultrafiltration membranes. Upon flash welding, both conductivity and pure water permeability of the membranes improves by nearly a factor of 10, while maintaining silica nanoparticle rejection levels above 90%. Flash welding of SWCNT-PANi composite membranes holds promise for formation of electrochemically tunable membranes. PMID:23525119

  11. Exposure and Emissions Monitoring during Carbon Nanofiber Production—Part I: Elemental Carbon and Iron–Soot Aerosols

    PubMed Central

    Birch, M. Eileen; Ku, Bon-Ki; Evans, Douglas E.; Ruda-Eberenz, Toni A.

    2015-01-01

    Production of carbon nanofibers and nanotubes (CNFs/CNTs) and their composite products is increasing globally. High volume production may increase the exposure risks for workers who handle these materials. Though health effects data for CNFs/CNTs are limited, some studies raise serious health concerns. Given the uncertainty about their potential hazards, there is an immediate need for toxicity data and field studies to assess exposure to CNFs/CNTs. An extensive study was conducted at a facility that manufactures and processes CNFs. Filter, sorbent, cascade impactor, bulk, and microscopy samples, combined with direct-reading instruments, provided complementary information on air contaminants. Samples were analyzed for organic carbon (OC) and elemental carbon (EC), metals, and polycyclic aromatic hydrocarbons (PAHs), with EC as a measure of CNFs. Transmission electron microscopy with energy-dispersive X-ray spectroscopy also was applied. Fine/ultrafine iron-rich soot, PAHs, and carbon monoxide were production byproducts. Direct-reading instrument results were reported previously [Evans DE et al. (Aerosol monitoring during carbon nanofiber production: mobile direct-reading sampling. Ann Occup Hyg 2010;54:514–31.)] Results for time-integrated samples are reported as companion papers in this Issue. OC and EC, metals, and microscopy results are reported here, in Part I, while results for PAHs are reported in Part II [Birch ME. (Exposure and Emissions Monitoring during Carbon Nanofiber Production—Part II: Polycyclic Aromatic Hydrocarbons. Ann. Occup. Hyg 2011; 55: 1037–47.)]. Respirable EC area concentrations inside the facility were about 6–68 times higher than outdoors, while personal breathing zone samples were up to 170 times higher. PMID:21965464

  12. Diamond synthesis from carbon nanofibers at low temperature and low pressure

    PubMed Central

    Luo, Chengzhi; Qi, Xiang; Pan, Chunxu; Yang, Wenge

    2015-01-01

    In this article, we report a new route to synthesize diamond by converting “solid” carbon nanofibers with a Spark Plasma Sintering system under low temperature and pressure (even at atmospheric pressure). Well-crystallized diamond crystals are obtained at the tips of the carbon nanofibers after sintering at 1500 °C and atmospheric pressure. Combining with scanning electron microscopy, transmission electron microscopy, electron-energy loss spectroscopy and Raman spectroscopy observations, we propose the conversion mechanism as follows: the disorder “solid” carbon nanofibers → well crystallined carbon nanofibers → bent graphitic sheets → onion-liked rings → diamond single crystal → the bigger congregated diamond crystal. It is believed that the plasma generated by low-voltage, vacuum spark, via a pulsed DC in Spark Plasma Sintering process, plays a critical role in the low temperature and low pressure diamond formation. This Spark Plasma Sintering process may provide a new route for diamond synthesis in an economical way to a large scale. PMID:26351089

  13. Diamond synthesis from carbon nanofibers at low temperature and low pressure

    NASA Astrophysics Data System (ADS)

    Luo, Chengzhi; Qi, Xiang; Pan, Chunxu; Yang, Wenge

    2015-09-01

    In this article, we report a new route to synthesize diamond by converting “solid” carbon nanofibers with a Spark Plasma Sintering system under low temperature and pressure (even at atmospheric pressure). Well-crystallized diamond crystals are obtained at the tips of the carbon nanofibers after sintering at 1500 °C and atmospheric pressure. Combining with scanning electron microscopy, transmission electron microscopy, electron-energy loss spectroscopy and Raman spectroscopy observations, we propose the conversion mechanism as follows: the disorder “solid” carbon nanofibers → well crystallined carbon nanofibers → bent graphitic sheets → onion-liked rings → diamond single crystal → the bigger congregated diamond crystal. It is believed that the plasma generated by low-voltage, vacuum spark, via a pulsed DC in Spark Plasma Sintering process, plays a critical role in the low temperature and low pressure diamond formation. This Spark Plasma Sintering process may provide a new route for diamond synthesis in an economical way to a large scale.

  14. Diamond synthesis from carbon nanofibers at low temperature and low pressure.

    PubMed

    Luo, Chengzhi; Qi, Xiang; Pan, Chunxu; Yang, Wenge

    2015-01-01

    In this article, we report a new route to synthesize diamond by converting "solid" carbon nanofibers with a Spark Plasma Sintering system under low temperature and pressure (even at atmospheric pressure). Well-crystallized diamond crystals are obtained at the tips of the carbon nanofibers after sintering at 1500 °C and atmospheric pressure. Combining with scanning electron microscopy, transmission electron microscopy, electron-energy loss spectroscopy and Raman spectroscopy observations, we propose the conversion mechanism as follows: the disorder "solid" carbon nanofibers→well crystallined carbon nanofibers→bent graphitic sheets→onion-liked rings→diamond single crystal→the bigger congregated diamond crystal. It is believed that the plasma generated by low-voltage, vacuum spark, via a pulsed DC in Spark Plasma Sintering process, plays a critical role in the low temperature and low pressure diamond formation. This Spark Plasma Sintering process may provide a new route for diamond synthesis in an economical way to a large scale. PMID:26351089

  15. Hierarchically porous carbon nanosheets from waste coffee grounds for supercapacitors.

    PubMed

    Yun, Young Soo; Park, Min Hong; Hong, Sung Ju; Lee, Min Eui; Park, Yung Woo; Jin, Hyoung-Joon

    2015-02-18

    The nanostructure design of porous carbon-based electrode materials is key to improving the electrochemical performance of supercapacitors. In this study, hierarchically porous carbon nanosheets (HP-CNSs) were fabricated using waste coffee grounds by in situ carbonization and activation processes using KOH. Despite the simple synthesis process, the HP-CNSs had a high aspect ratio nanostructure (∼20 nm thickness to several micrometers in lateral size), a high specific surface area of 1945.7 m(2) g(-1), numerous heteroatoms, and good electrical transport properties, as well as hierarchically porous characteristics (0.5-10 nm in size). HP-CNS-based supercapacitors showed a specific energy of 35.4 Wh kg(-1) at 11250 W kg(-1) and of 23 Wh kg(-1) for a 3 s charge/discharge current rate corresponding to a specific power of 30000 W kg(-1). Additionally, the HP-CNS supercapacitors demonstrated good cyclic performance over 5000 cycles. PMID:25612009

  16. The effect of filler aspect ratio on the electromagnetic properties of carbon-nanofibers reinforced composites

    SciTech Connect

    De Vivo, B.; Lamberti, P.; Spinelli, G. Tucci, V.; Guadagno, L.; Raimondo, M.

    2015-08-14

    The effect of filler aspect ratio on the electromagnetic properties of epoxy-amine resin reinforced with carbon nanofibers is here investigated. A heat treatment at 2500 °C of carbon nanofibers seems to increase their aspect ratio with respect to as-received ones most likely due to a lowering of structural defects and the improvement of the graphene layers within the dixie cup conformation. These morphological differences revealed by Raman's spectroscopy and scanning electron microscopy analyses may be responsible for the different electrical properties of the resulting composites. The DC characterization of the nanofilled material highlights an higher electrical conductivity and a lower electrical percolation threshold for the heat-treated carbon nanofibers based composites. In fact, the electrical conductivity is about 0.107 S/m and 1.36 × 10{sup −3} S/m for the nanocomposites reinforced with heat-treated and as received fibers, respectively, at 1 wt. % of nanofiller loading, while the electrical percolation threshold falls in the range [0.05–0.32]wt. % for the first nanocomposites and above 0.64 wt. % for the latter. Moreover, also a different frequency response is observed since the critical frequency, which is indicative of the transition from a resistive to a capacitive-type behaviour, shifts forward of about one decade at the same filler loading. The experimental results are supported by theoretical and simulation studies focused on the role of the filler aspect ratio on the electrical properties of the nanocomposites.

  17. Performance Evaluation of Activated Carbon Nanofiber as Carbon Supports to Improve the Cyclability of Li-Air Batteries.

    PubMed

    Park, Inyeong; Kim, Heeyun; Shim, Sang Eun; Baeck, Sung-Hyeon

    2015-11-01

    This study addresses the effects of the pore structures of carbon materials used as cathodes for non-aqueous lithium-air batteries on cycle life. Carbon Nanofibers (CNFs) were synthesized by electrospinning polyacrylonitrile (PAN) and carbonization. The synthesized CNF was then converted to activated carbon nanofibers (ACNFs) under flowing CO2. The specific surface areas CNFs were increased on activation. ACNFs were arranged randomly to form a web-like structure providing both oxygen pathways and a means of discharging products. To examine the electrochemical properties of ACNF, charge-discharge tests were conducted using a Swagelok-type cell at a constant current density of 0.2 mA/cm2; impedance tests were also conducted. ACNF sheet electrodes had cycle lives of up to 50 cycles, which was attributed to high surface area and porosity, although overpotentials for both charge and discharge were high. This cycling performance showed that the pore structure of sheet ACNF is more suitable for the transport of oxygen and for the storage of discharge products than carbon powders. PMID:26726643

  18. Controlled Growth of NiCo2O4 Nanorods and Ultrathin Nanosheets on Carbon Nanofibers for High-performance Supercapacitors

    PubMed Central

    Zhang, Genqiang; (David) Lou, Xiong Wen

    2013-01-01

    Two one-dimensional hierarchical hybrid nanostructures composed of NiCo2O4 nanorods and ultrathin nanosheets on carbon nanofibers (CNFs) are controllably synthesized through facile solution methods combined with a simple thermal treatment. The structure of NiCo2O4 can be easily controlled to be nanorods or nanosheets by using different additives in the synthesis. These two different nanostructures are evaluated as electrodes for high performance supercapacitors, in view of their apparent advantages, such as high electroactive surface area, ultrathin and porous features, robust mechanical strength, shorter ion and electron transport path. Their electrochemical performance is systematically studied, and both of these two hierarchical hybrid nanostructures exhibit high capacitance and excellent cycling stability. The remarkable electrochemical performance will undoubtedly make these hybrid structures attractive for high-performance supercapacitors with high power and energy densities. PMID:23503561

  19. Effects of ligand monolayers on catalytic nickel nanoparticles for synthesizing vertically aligned carbon nanofibers

    SciTech Connect

    Sarac, Mehmet; Robert, Wilson; Johnsont-Peck, Aaron; Wang, Junwei; Pearce, Ryan; Klein, Kate; Melechko, Anatoli; Tracy, Joseph

    2011-03-01

    Vertically aligned carbon nanofibers (VACNFs) were synthesized using ligand-stabilized Ni nanoparticle (NP) catalysts and plasmaenhanced chemical vapor deposition. Using chemically synthesized Ni NPs enables facile preparation of VACNF arrays with monodisperse diameters below the size limit of thin film lithography. During pregrowth heating, the ligands catalytically convert into graphitic shells that prevent the catalyst NPs from agglomerating and coalescing, resulting in a monodisperse VACNF size distribution. In comparison, significant agglomeration occurs when the ligands are removed before VACNF growth, giving a broad distribution of VACNF sizes. The ligand shells are also promising for patterning the NPs and synthesizing complex VACNF arrays.

  20. Plum-branch-like carbon nanofibers decorated with SnO2 nanocrystals

    NASA Astrophysics Data System (ADS)

    Yang, Zunxian; Du, Guodong; Guo, Zaiping; Yu, Xuebin; Li, Sean; Chen, Zhixin; Zhang, Peng; Liu, Huakun

    2010-06-01

    Novel plum-branch-like carbon nanofibers (CNFs) decorated with SnO2 nanocrystals have been synthesized by electrospinning and subsequent thermal treatment in an Ar/H2O atmosphere. The morphologies of the as-synthesized SnO2/CNF composites and the contents of carbon and SnO2 can be controlled by adjusting the heat treatment temperature. It is proposed that the growth of SnO2/CNF composites follows the outward diffusion of tin composites from the as-spun tin composite/polyacrylonitrile (PAN) nanofibers, pyrolysis of PAN and oxidation of tin composites, and then formation of SnO2 nanocrystals around the CNFs. This novel 1D SnO2/CNF composite may have potential application in nanobatteries, nano fuel cells, and nanosensors. A preliminary result has revealed that the SnO2/CNF composite presents favourable electrochemical performance in lithium-ion batteries.Novel plum-branch-like carbon nanofibers (CNFs) decorated with SnO2 nanocrystals have been synthesized by electrospinning and subsequent thermal treatment in an Ar/H2O atmosphere. The morphologies of the as-synthesized SnO2/CNF composites and the contents of carbon and SnO2 can be controlled by adjusting the heat treatment temperature. It is proposed that the growth of SnO2/CNF composites follows the outward diffusion of tin composites from the as-spun tin composite/polyacrylonitrile (PAN) nanofibers, pyrolysis of PAN and oxidation of tin composites, and then formation of SnO2 nanocrystals around the CNFs. This novel 1D SnO2/CNF composite may have potential application in nanobatteries, nano fuel cells, and nanosensors. A preliminary result has revealed that the SnO2/CNF composite presents favourable electrochemical performance in lithium-ion batteries. Electronic supplementary information (ESI) available: Figures S1-S6. See DOI: 10.1039/c0nr00009d

  1. Cu grown carbon nanofibers - Variation of their chemical and physical properties

    NASA Astrophysics Data System (ADS)

    Bhoware, Shrikant; Maubane, Manoko S.; Phaahlamohlaka, Tumelo; Shaikjee, Ahmed; Coville, Neil J.

    2013-07-01

    Carbon nanofibers (CNFs) were prepared by passing a mixture of acetylene/H2 or acetylene/N2 over different Cu catalysts. The Soxhlet extracted CNFs were characterized by TEM, TGA and IR spectroscopy and revealed that the morphology, diameter distribution and crystallinity of the CNFs varied with gas atmosphere and Cu particle size. TEM images revealed that coiled CNFs were only produced from Cu/SiO2 grown in the presence of H2. It is thus revealed that the CNFs produced by different Cu catalysts have different chemical and physical properties and that these properties correlate with catalyst particle size and the gas mixtures used.

  2. CdS loaded on coal based activated carbon nanofibers with enhanced photocatalytic property

    NASA Astrophysics Data System (ADS)

    Guo, Jixi; Guo, Mingxi; Jia, Dianzeng; Song, Xianli; Tong, Fenglian

    2016-08-01

    The coal based activated carbon nanofibers (CBACFs) were prepared by electrospinning a mixture of polyacrylonitrile (PAN) and acid treated coal. Cadmium sulfide (CdS) nanoparticles loaded on CBACFs were fabricated by solvothermal method. The obtained samples were characterized by FESEM, TEM, and XRD. The results reveal that the CdS nanoparticles are homogeneously dispersed on the surfaces of CBACFs. The CdS/CBACFs nanocomposites exhibited higher photoactivity for photodegradation of methyl blue (MB) under visible light irradiation than pure CdS nanoparticles. CBACFs can be used as low cost support materials for the preparation of nanocomposites with high photocatalytic activity.

  3. WO3-x Nanoplates Grown on Carbon Nanofibers for an Efficient Electrocatalytic Hydrogen Evolution Reaction.

    PubMed

    Chen, JiaDong; Yu, DanNi; Liao, WeiSha; Zheng, MengDan; Xiao, LongFei; Zhu, Han; Zhang, Ming; Du, MingLiang; Yao, JuMing

    2016-07-20

    The search for non-noble metal catalysts with high activity for the hydrogen evolution reaction (HER) is crucial for efficient hydrogen production at low cost and on a large scale. Herein, we report a novel WO3-x catalyst synthesized on carbon nanofiber mats (CFMs) by electrospinning and followed by a carbonization process in a tubal furnace. The morphology and composition of the catalysts were tailored via a simple method, and the hybrid catalyst mats were used directly as cathodes to investigate their HER performance. Notably, the as-prepared catalysts exhibit substantially enhanced activity for the HER, demonstrating a small overpotential, a high exchange current density, and a large cathodic current density. The remarkable electrocatalytic performances result from the poor crystallinity of WO3-x, the high electrical conductivity of WO3-x, and the use of electrospun CNFs. The present work outlines a straightforward approach for the synthesis of transition metal oxide (TMO)-based carbon nanofiber mats with promising applications for the HER. PMID:27356101

  4. Thermal decomposition of alkane hydrocarbons inside a porous Ni anode for fuel supply of direct carbon fuel cell: Effects of morphology and crystallinity of carbon

    NASA Astrophysics Data System (ADS)

    Li, Chengguo; Yi, Hakgyu; Jalalabadi, Tahereh; Lee, Donggeun

    2015-10-01

    This study improved the physical contact between anode and fuel in a direct carbon fuel cell (DCFC) by directly generating carbon in a porous Ni anode through thermal decomposition of three kinds of hydrocarbons (CH4, C2H6, C3H8). From electron microscope observations of the carbon particles generated from each hydrocarbon, carbon spheres (CS), carbon nanotubes (CNT) and carbon nanofibers (CNF) were identified with increasing carbon number. Raman scattering analysis was performed to determine the crystallinity of the carbon samples. As a result, the carbon samples (CS, CNT, and CNF) produced from CH4, C2H6 and C3H8 were found to be less crystalline and more flexible with increasing the carbon number. DCFC performance was measured at 700 °C for the anode fueled with the same mass of the carbon sample. It was found that the 1-dimensional CNT and CNF were more active to produce 148% and 210% times higher power density than the CS. The difference was partly attributed to the finding that the less-crystalline CNT and CNF had much lower charge transfer resistances than the CS. A lifetime test found that the CNT and CNF, which are capable of transporting electrons for much longer periods, maintained the power density much longer, as compared to the CS which can lose their point contacts between the particles shortly at high current density.

  5. Tin nanoparticles encapsulated in porous multichannel carbon microtubes: preparation by single-nozzle electrospinning and application as anode material for high-performance Li-based batteries.

    PubMed

    Yu, Yan; Gu, Lin; Zhu, Changbao; van Aken, Peter A; Maier, Joachim

    2009-11-11

    Tin nanoparticles encapsulated in porous multichannel carbon microtubes (denoted as SPMCTs) were prepared by carbonization of electrospun PAN-PMMA-tin octoate nanofibers fabricated using a single-nozzle electrospinning technique. This material exhibited excellent characteristics for lithium ion battery anode applications in terms of reversible capacities, cycling performance, and rate capability. Undertaking such a production configuration allows the long-existing problem of obtaining a high packing density of tin particles while retaining sufficient spare space to buffer the volume variation during lithium alloying and dealloying processes to be properly addressed. Furthermore, the porous carbon shell preserves both the mechanical and chemical stability of the function-active Sn metal, which also serves as a highly conductive medium allowing Li(+) to access. PMID:19886691

  6. Novel strategy for the synthesis of vertically orientated carbon nanofibers

    SciTech Connect

    Perez-Cabero, M.; Kuvshinov, D.; Guerrero-Ruiz, A.; Rodriguez-Ramos, I.

    2008-07-01

    This paper presents a first approach of a simple way to obtain vertically orientated carbon nanotubes. The used catalytic system consisted of quartz or graphite plates, on which some iron solutions (of precursors such as nitrates or phthalocyanines) were deposited by simple impregnation, generating homogeneous films. After drying, the plates were submitted to reduction and reaction procedure, which consisted in acetylene decomposition at 750 deg. C during 1 h. Samples after reaction were studied by scanning electron microscopy and transmission electron microscopy, which confirmed the formation of homogeneous and vertically orientated structures of carbon nanotubes over the plates.

  7. Magnetic properties of NiFe2O4/carbon nanofibers from Venezuelan petcoke

    NASA Astrophysics Data System (ADS)

    Briceño, Sarah; Silva, Pedro; Molina, Wilmer; Brämer-Escamilla, Werner; Alcalá, Olgi; Cañizales, Edgard

    2015-05-01

    NiFe2O4/carbon nanofibers (NiFe2O4/CNFs) have been successfully synthesized by hydrotermal method using Venezuelan petroleum coke (petcoke) as carbon source and NiFe2O4 as catalyst. The morphology, structural and magnetic properties of nanocomposite products were characterized by X-ray diffraction (XRD), high-resolution transmission electron microscopy (HR-TEM), vibrating sample magnetometry (VSM) and electron paramagnetic resonance (EPR). XRD analysis revealed a cubic spinel structure and ferrite phase with high crystallinity. HR-TEM reveals the presence of CNFs with diameters of 4±2 nm. At room temperature, NiFe2O4/CNFs show superparamagnetic behavior with a maximum magnetization of 15.35 emu/g. Our findings indicate that Venezuelan petroleum coke is suitable industrial carbon source for the growth of magnetic CNFs.

  8. Properties that Influence the Specific Surface Areas of Carbon Nanotubes and Nanofibers

    PubMed Central

    BIRCH, M. EILEEN; RUDA-EBERENZ, TONI A.; CHAI, MING; ANDREWS, RONNEE; HATFIELD, RANDAL L.

    2015-01-01

    Commercially available carbon nanotubes and nanofibers were analyzed to examine possible relationships between their Brunauer–Emmett–Teller specific surface areas (SSAs) and their physical and chemical properties. Properties found to influence surface area were number of walls/diameter, impurities, and surface functionalization with hydroxyl and carboxyl groups. Characterization by electron microscopy, energy-dispersive X-ray spectrometry, thermogravimetric analysis, and elemental analysis indicates that SSA can provide insight on carbon nanomaterials properties, which can differ vastly depending on synthesis parameters and post-production treatments. In this study, how different properties may influence surface area is discussed. The materials examined have a wide range of surface areas. The measured surface areas differed from product specifications, to varying degrees, and between similar products. Findings emphasize the multiple factors that influence surface area and mark its utility in carbon nanomaterial characterization, a prerequisite to understanding their potential applications and toxicities. Implications for occupational monitoring are discussed. PMID:24029925

  9. A reagentless enzymatic amperometric biosensor using vertically aligned carbon nanofibers (VACNF)

    SciTech Connect

    Weeks, Martha L; Rahman, Touhidur; Frymier, Paul Dexter; Islam, Syed K; McKnight, Timothy E

    2008-01-01

    A reagentless amperometric enzymatic biosensor is constructed on a carbon substrate for detection of ethanol. Yeast alcohol dehydrogenase (YADH), an oxidoreductase, and its cofactor nicotinamide adenine dinucleotide (NAD+) are immobilized by adsorption and covalent attachment to the carbon substrate. Carbon nanofibers grown by plasma enhanced chemical vapor deposition (PECVD) are chosen as the electrode material due to their excellent structural and electrical properties. Electrochemical techniques are employed to test the functionality and performance of the biosensor using reduced form of nicotinamide adenine dinucleotide (NADH) which also determines the oxidation peak potential of NADH. Subsequently, amperometric measurements are conducted for detection of ethanol to determine the electrical current response due to the increase in analyte concentration. The detection range, storage stability, reusability, and response time of the biosensor are also examined.

  10. Design and evaluation of carbon nanofiber and silicon materials for neural implant applications

    NASA Astrophysics Data System (ADS)

    McKenzie, Janice L.

    Reduction of glial scar tissue around central nervous system implants is necessary for improved efficacy in chronic applications. Design of materials that possess tunable properties inspired by native biological tissue and elucidation of pertinent cellular interactions with these materials was the motivation for this study. Since nanoscale carbon fibers possess the fundamental dimensional similarities to biological tissue and have attractive material properties needed for neural biomaterial implants, this present study explored cytocompatibility of these materials as well as modifications to traditionally used silicon. On silicon materials, results indicated that nanoscale surface features reduced astrocyte functions, and could be used to guide neurite extension from PC12 cells. Similarly, it was determined that astrocyte functions (key cells in glial scar tissue formation) were reduced on smaller diameter carbon fibers (125 nm or less) while PC12 neurite extension was enhanced on smaller diameter carbon fibers (100 nm or less). Further studies implicated laminin adsorption as a key mechanism in enhancing astrocyte adhesion to larger diameter fibers and at the same time encouraging neurite extension on smaller diameter fibers. Polycarbonate urethane (PCU) was then used as a matrix material for the smaller diameter carbon fibers (100 and 60 nm). These composites proved very versatile since electrical and mechanical properties as well as cell functions and directionality could be influenced by changing bulk and surface composition and features of these matrices. When these composites were modified to be smooth at the micronscale and only rough at the nanoscale, P19 cells actually submerged philopodia, extensions, or whole cells bodies beneath the PCU in order to interact with the carbon nanofibers. These carbon nanofiber composites that have been formulated are a promising material to coat neural probes and thereby enhance functionality at the tissue interface. This

  11. Sorption of pollutants by porous carbon, carbon nanotubes and fullerene- an overview.

    PubMed

    Gupta, Vinod K; Saleh, Tawfik A

    2013-05-01

    The quality of water is continuously deteriorating due to its increasing toxic threat to humans and the environment. It is imperative to perform treatment of wastewater in order to remove pollutants and to get good quality water. Carbon materials like porous carbon, carbon nanotubes and fullerene have been extensively used for advanced treatment of wastewaters. In recent years, carbon nanomaterials have become promising adsorbents for water treatment. This review attempts to compile relevant knowledge about the adsorption activities of porous carbon, carbon nanotubes and fullerene related to various organic and inorganic pollutants from aqueous solutions. A detailed description of the preparation and treatment methods of porous carbon, carbon nanotubes and fullerene along with relevant applications and regeneration is also included. PMID:23430732

  12. Improving microstructure of silicon/carbon nanofiber composites as a Li battery anode

    SciTech Connect

    Howe, Jane Y; Meyer III, Harry M; Burton, David J.; Qi, Dr. Yue; Nazri, Maryam; Nazri, G. Abbas; Palmer, Andrew C.; Lake, Patrick D.

    2013-01-01

    We report the interfacial study of a silicon/carbon nanofiber (Si/CNF) nanocomposite material as a potentially high performance anode for rechargeable lithium ion batteries. The carbon nanofiber is hollow, with a graphitic interior and turbostratic exterior. Amorphous silicon layers were uniformly coated via chemical vapor deposition on both the exterior and interior surfaces of the CNF. The resulting Si/CNF composites were tested as anodes for Li ion batteries and exhibited capacities near 800 mAh g1 for 100 cycles. After cycling, we found that more Si had fallen off from the outer wall than from the innerwall of CNF. Theoretical calculations confirmed that this is due to a higher interfacial strength at the Si/Cedge interface at the inner wall than that of the Si/C-basal interface at the outer wall. Based upon the experimental analysis and theoretical calculation, we have proposed several interfacial engineering approaches to improve the performance of the electrodes by optimizing the microstructure of this nanocomposite.

  13. Activated carbon nanofibers (ACNF) as cathode for single chamber microbial fuel cells (SCMFCs)

    NASA Astrophysics Data System (ADS)

    Santoro, Carlo; Stadlhofer, Astrid; Hacker, Viktor; Squadrito, Gaetano; Schröder, Uwe; Li, Baikun

    2013-12-01

    The suitability of carbon nanofibers (CNF) based cathodes as alternative to the platinum (Pt)-based cathode in single chamber microbial fuel cells (SCMFCs) were extensively studied over 3-month operational period. MFCs were fed with two solutions: synthetic wastewater (phosphate buffer (PBS) plus sodium acetate) and real wastewater (mixed liquor suspendedsolid (MLSS) solution). CNFs were chemically activated using HNO3 and then hot pressed on a carbon cloth support to increase surface area. The cathode polarization showed a better behavior of the clean Pt-based cathode in abiotic conditions. The activation of the nanofibers (ACNFs) gave an advantage to the cathode performances compared to the raw CNFs. The SCMFCs fed with PBS showed four times higher power generation compared to MLSS solution. All the cathodes showed a decrease in performances over time, and the advantage of the Pt over CNF/ACNF disappeared. CNF/ACNF cathodes showed more stability in performances in long time operations. Biofilm formation, salt precipitations on the cathode, and the presence of hydrogen sulfide decreased the activity of Pt cathodes. A degradation and Pt detachment were noticed on Pt cathodes over time. In contrast, CNF/ACNF cathodes exhibited less deterioration throughout the operational period, which demonstrated a great potential as cost-effective cathodes for long-term operation.

  14. Nanocomposite of Au Nanoparticles/Helical Carbon Nanofibers and Application in Hydrogen Peroxide Biosensor.

    PubMed

    Zhai, Mumu; Cui, Rongjing; Gu, Ning; Zhang, Genhua; Lin, Wang; Yu, Lingjun

    2015-06-01

    A combined sol-gel/hydrogen reduction method has been developed for the mass production of helical carbon nanofibers (HCNFs) by the pyrolysis of acetylene at 425 degrees C in the presence of NiO nanoparticles. The synthesized HCNFs were characterized with scanning electron microscopy (SEM), X-ray diffraction (XRD) and high resolution transmission electron microscopy (HRTEM). The helical-structured carbon nanofibers have a large specific surface area and excellent biocompatibility. A novel enzymatic hydrogen peroxide sensor was then successfully fabricated based on the nanocomposites containing HCNFs and gold nanoparticles (AuNPs). The results indicated that the Au/HCNFs nanocomposites exhibited excellent electrocatalytic activity to the reduction of H2O2, offering a wide linear range from 1.0 μM to 3157 μM with a detection limit as low as 0.46 μM. The apparent Michaelis-Menten constant of the biosensor was 0.61 mM. The as-fabricated biosensor showed a rapid and sensitive amperometric response to hydrogen peroxide with acceptable preparation reproducibility and excellent stability. Because of their low cost and high stability, these novel HCNFs represent seem to be a kind of promising biomaterial and may find wide new applications in scopes such as biocatalysis, immunoassay, environmental monitoring and so on. PMID:26369097

  15. Superhydrophobic and conductive carbon nanofiber/PTFE composite coatings for EMI shielding.

    PubMed

    Das, Arindam; Hayvaci, Harun T; Tiwari, Manish K; Bayer, Ilker S; Erricolo, Danilo; Megaridis, Constantine M

    2011-01-01

    This paper presents a solvent-based, mild method to prepare superhydrophobic, carbon nanofiber/PTFE-filled polymer composite coatings with high electrical conductivity and reports the first data on the effectiveness of such coatings as electromagnetic interference (EMI) shielding materials. The coatings are fabricated by spraying dispersions of carbon nanofibers and sub-micron PTFE particles in a polymer blend solution of poly(vinyledene fluoride) and poly(methyl methacrylate) on cellulosic substrates. Upon drying, coatings display static water contact angles as high as 158° (superhydrophobic) and droplet roll-off angles of 10° indicating self-cleaning ability along with high electrical conductivities (up to 309 S/m). 100 μm-thick coatings are characterized in terms of their EMI shielding effectiveness in the X-band (8.2-12.4 GHz). Results show up to 25 dB of shielding effectiveness, which changed little with frequency at a fixed composition, thus indicating the potential of these coatings for EMI shielding applications and other technologies requiring both extreme liquid repellency and high electrical conductivity. PMID:20889160

  16. Label-free detection of C-reactive protein using a carbon nanofiber based biosensor

    PubMed Central

    Gupta, Rakesh K.; Periyakaruppan, Adaikkappan; Meyyappan, M.; Koehne, Jessica E.

    2014-01-01

    We report the sensitive detection of C-reactive protein (CRP), a biomarker for cardiac disease, using a carbon nanofiber based biosensor platform. Vertically aligned carbon nanofibers were grown using plasma enhanced chemical vapor deposition to fabricate nanoelectrode arrays in a 3 X 3 configuration. Cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS) were used for the CRP detection. The CV responses show a 25 % reduction in redox current upon the immobilization of anti-CRP on the electrode where as a 30% increase in charge transfer resistance is seen from EIS. Further reduction in redox current and increase in charge transfer resistance result from binding of CRP on anti-CRP immobilized surface, proportional to the concentration of the CRP target. The detection limit of the sensor is found to be ~90 pM or ~11 ng/ml, which is in the clinically relevant range. Control tests using non-specific myoglobin antigen confirmed the specificity of the present approach. PMID:24709327

  17. Effect of carbon nanofiber surface functional groups on oxygen reduction in alkaline solution

    NASA Astrophysics Data System (ADS)

    Zhong, Ren-Sheng; Qin, Yuan-Hang; Niu, Dong-Fang; Tian, Jing-Wei; Zhang, Xin-Sheng; Zhou, Xin-Gui; Sun, Shi-Gang; Yuan, Wei-Kang

    2013-03-01

    Carbon nanofibers (CNFs) with different content of surface functional groups which are carboxyl groups (CNF-OX), carbonyl groups (CNF-CO) and hydroxyl groups (CNF-OH) and nitrogen-containing groups (CNF-ON) are synthesized, and their electrocatalytic activities toward oxygen reduction reaction (ORR) in alkaline solution are investigated. The result of X-ray photoelectron spectroscopy (XPS) characterization indicates that a higher concentration of carboxyl groups, carbonyl groups and hydroxyl groups are imported onto the CNF-OX, CNF-CO and CNF-OH, respectively. Cyclic voltammetry shows that both the oxygen- and nitrogen-containing groups can improve the electrocatalytic activity of CNFs for ORR. The CNF-ON/GC electrode, which has nitrogen-containing groups, exhibits the highest current density of ORR. Rotating disk electrode (RDE) characterization shows that the oxygen reduction on CNF-ON/GC electrode proceeds almost entirely through the four-electron reduction pathway, the CNF-OX/GC, CNF-CO/GC and CNF-OH/GC electrodes proceed a two-electron reduction pathway at low potentials (-0.2 V to -0.6 V) followed by a gradual four-electron reduction pathway at more negative potentials, while the untreated carbon nanofiber (CNF-P/GC) electrode proceeds predominantly by a two-electron reduction pathway within the whole range of potential studied.

  18. Fabrication and Characterization of High Temperature Resin/Carbon Nanofiber Composites

    NASA Technical Reports Server (NTRS)

    Ghose, Sayata; Watson, Kent A.; Working, Dennis C.; Criss, Jim M.; Siochi, Emilie J.; Connell, John W.

    2005-01-01

    Multifunctional composites present a route to structural weight reduction. Nanoparticles such as carbon nanofibers (CNF) provide a compromise as a lower cost nanosize reinforcement that yields a desirable combination of properties. Blends of PETI-330 and CNFs were prepared and characterized to investigate the potential of CNF composites as a high performance structural medium. Dry mixing techniques were employed and the effect of CNF loading level on melt viscosity was determined. The resulting powders were characterized for degree of mixing, thermal and rheological properties. Based on the characterization results, samples containing 30 and 40 wt% CNF were scaled up to approx.300 g and used to fabricate moldings 10.2 cm x 15.2 cm x 0.32 cm thick. The moldings were fabricated by injecting the mixtures at 260-280 C into a stainless steel tool followed by curing for 1 h at 371 C. The tool was designed to impart high shear during the process in an attempt to achieve some alignment of CNFs in the flow direction. Moldings were obtained that were subsequently characterized for thermal, mechanical and electrical properties. The degree of dispersion and alignment of CNFs were investigated using high-resolution scanning electron microscopy. The preparation and preliminary characterization of PETI-330/CNF composites are discussed. Keywords: resins, carbon nanofibers, scanning electron microscopy, electrical properties, thermal conductivity,injection

  19. Carbon nanofiber electrodes and controlled nanogaps for scanning electrochemical microscopy experiments.

    PubMed

    Tel-Vered, Ran; Walsh, Darren A; Mehrgardi, Masoud A; Bard, Allen J

    2006-10-01

    The electrochemical behavior of electrodes made by sealing carbon nanofibers in glass or with electrophoretic paint has been studied by scanning electrochemical microscopy (SECM). Because of their small electroactive surface area, conical geometry with a low aspect ratio and high overpotential for proton and oxygen reduction, carbon nanofiber (CNF) electrodes are promising candidates for producing electrode nanogaps, imaging with high spatial resolution and for the electrodeposition of single metal nanoparticles (e.g., Pt, Pd) for studies as electrocatalysts. By using the feedback mode of the SECM, a CNF tip can produce a gap that is smaller than 20 nm from a platinum disk. Similarly, the SECM used in a tip-collection substrate-generation mode, which subsequently shows a feedback interaction at short distances, makes it possible to detect a single CNF by another CNF and then to form a nanometer gap between the two electrodes. This approach was used to image vertically aligned CNF arrays. This method is useful in the detection in a homogeneous solution of short-lifetime intermediates, which can be electrochemically generated at one electrode and collected at the second at distances that are equivalent to a nanosecond time scale. PMID:17007521

  20. Improving Microstructure of Silicon/Carbon Nanofiber Composites as A Li Battery Anode

    SciTech Connect

    Howe, Jane Y; Burton, David J.; Meyer III, Harry M; Nazri, Maryam; Nazri, G. Abbas; Palmer, Andrew C.; Lake, Patrick D.

    2013-01-01

    We report the interfacial study of a silicon/carbon nanofiber (Si/CNF) nanocomposite material as a potentially high performance anode for rechargeable lithium ion batteries. The carbon nanofiber is hollow, with a graphitic interior and turbostratic exterior. Amorphous silicon layers were uniformly coated via chemical vapor deposition on both the exterior and interior surfaces of the CNF. The resulting Si/CNF composites were tested as anodes for Li ion batteries and exhibited capacities near 800 mAh g{sup -1} for 100 cycles. After cycling, we found that more Si had fallen off from the outer wall than from the inner wall of CNF. Theoretical calculations confirmed that this is due to a higher interfacial strength at the Si/C-edge interface at the inner wall than that of the Si/C-basal interface at the outer wall. Based upon the experimental analysis and theoretical calculation, we have proposed several interfacial engineering approaches to improve the performance of the electrodes by optimizing the microstructure of this nanocomposite.

  1. Synthesis, characterization and hydrogen storage studies on porous carbon

    SciTech Connect

    Ruz, Priyanka Banerjee, Seemita; Sudarsan, V.; Pandey, M.

    2015-06-24

    Porous carbon sample has been prepared, using zeolite-Y as template followed by annealing at 800°C, with view to estimate the extent of hydrogen storage by the sample. Based on XRD, {sup 13}C MAS NMR and Raman spectroscopic studies it is confirmed that the porous Carbon sample contains only sp{sup 2} hybridized carbon. The hydrogen sorption isotherms have been recorded for the sample at 273, 223K and 123K and the maximum hydrogen absorption capacity is found to be 1.47wt% at 123K. The interaction energy of hydrogen with the carbon framework was determined to be ∼ 10 kJ mol{sup −1}at lower hydrogen uptake and gradually decreases with increase in hydrogen loading.

  2. XPS studies of Pt catalysts supported on porous carbon

    NASA Astrophysics Data System (ADS)

    Tyagi, Deepak; Varma, Salil; Bharadwaj, S. R.

    2016-05-01

    Pt catalysts supported on porous carbon were prepared by hard templating route and used for HI decomposition reaction of Sulfur Iodine thermochemical cycle. These catalysts were characterized by X-ray photoelectron spectroscopy for oxidation state of platinum as well as nature of carbon present in the catalysts. It was found that platinum is present in metallic state and carbon is present in both sp2 and sp3 hybridization states. The catalysts were evaluated for their activity and stability for liquid phase HI decomposition reaction and it was observed that mesoporous carbon based catalysts were more active and stable under the reaction conditions.

  3. Metastable carbon in two chondritic porous interplanetary dust particles

    NASA Technical Reports Server (NTRS)

    Rietmeijer, F. J. M.; Mackinnon, I. D. R.

    1986-01-01

    An understanding of carbonaceous matter in primitive extraterrestrial materials is an essential component of studies on dust evolution in the interstellar medium and the early history of the Solar System. Analytical Electron Microscopy (AEM) on carbonaceous material in two Chondritic Porous (CP) aggregrates is presented. The study suggests that a record of hydrocarbon carbonization may also be preserved in these materials.

  4. Porous Carbon Supports: Recent Advances with Various Morphologies and Compositions

    DOE PAGESBeta

    Zhang, Pengfei; Zhu, Huiyuan; Dai, Sheng

    2015-08-31

    The importance of porous carbon as the support material is well recognized in the catalysis community, and it would be even more attractive if several characteristics are considered, such as the stability in acidic and basic media or the ease of noble metal recovery through complete burn off. Because it is still difficult to obtain constant properties even from batch to batch, activated carbons are not popular in industrial catalysis now.

  5. Highly porous Zinc Stannate (Zn2SnO4) nanofibers scaffold photoelectrodes for efficient methyl ammonium halide perovskite solar cells.

    PubMed

    Mali, Sawanta S; Shim, Chang Su; Hong, Chang Kook

    2015-01-01

    Development of ternary metal oxide (TMO) based electron transporting layer (ETL) for perovskite solar cell open a new approaches toward efficient a unique strategy for solid state dye-sensitized solar cells (ssDSSCs). In the present investigation, highly porous zinc tin oxide (Zn2SnO4) scaffold nanofibers has been synthesized by electrospinning technique and successfully used for methyl ammonium lead halide (CH3NH3PbI3) perovskite sensitized solid state solar cells. The fabricated optimized perovskite solar cell devices exhibited 7.38% power conversion efficiency (PCE) with open circuit voltage (VOC) 0.986 V, current density (JSC) = 12.68 mAcm(-2) and fill factor (FF) 0.59 under AM 1.5 G sunlight (100 mWcm(-2)) which is higher than Zn2SnO4 nanoparticle (η = 2.52%) based perovskite solar cells. This improvement is achieved due to high porosity of Zn2SnO4 nanofibers and high crystallinity of the nanofibers synthesized at 700 °C. These results are remarkably higher than reported perovskite solar cells based on such type of ternary metal oxide ETLs. PMID:26094863

  6. Highly porous Zinc Stannate (Zn2SnO4) nanofibers scaffold photoelectrodes for efficient methyl ammonium halide perovskite solar cells

    PubMed Central

    Mali, Sawanta S.; Su Shim, Chang; Kook Hong, Chang

    2015-01-01

    Development of ternary metal oxide (TMO) based electron transporting layer (ETL) for perovskite solar cell open a new approaches toward efficient a unique strategy for solid state dye-sensitized solar cells (ssDSSCs). In the present investigation, highly porous zinc tin oxide (Zn2SnO4) scaffold nanofibers has been synthesized by electrospinning technique and successfully used for methyl ammonium lead halide (CH3NH3PbI3) perovskite sensitized solid state solar cells. The fabricated optimized perovskite solar cell devices exhibited 7.38% power conversion efficiency (PCE) with open circuit voltage (VOC) 0.986 V, current density (JSC) = 12.68 mAcm-2 and fill factor (FF) 0.59 under AM 1.5 G sunlight (100 mWcm−2) which is higher than Zn2SnO4 nanoparticle (η = 2.52%) based perovskite solar cells. This improvement is achieved due to high porosity of Zn2SnO4 nanofibers and high crystallinity of the nanofibers synthesized at 700 °C. These results are remarkably higher than reported perovskite solar cells based on such type of ternary metal oxide ETLs. PMID:26094863

  7. Highly porous Zinc Stannate (Zn2SnO4) nanofibers scaffold photoelectrodes for efficient methyl ammonium halide perovskite solar cells

    NASA Astrophysics Data System (ADS)

    Mali, Sawanta S.; Su Shim, Chang; Kook Hong, Chang

    2015-06-01

    Development of ternary metal oxide (TMO) based electron transporting layer (ETL) for perovskite solar cell open a new approaches toward efficient a unique strategy for solid state dye-sensitized solar cells (ssDSSCs). In the present investigation, highly porous zinc tin oxide (Zn2SnO4) scaffold nanofibers has been synthesized by electrospinning technique and successfully used for methyl ammonium lead halide (CH3NH3PbI3) perovskite sensitized solid state solar cells. The fabricated optimized perovskite solar cell devices exhibited 7.38% power conversion efficiency (PCE) with open circuit voltage (VOC) 0.986 V, current density (JSC) = 12.68 mAcm-2 and fill factor (FF) 0.59 under AM 1.5 G sunlight (100 mWcm-2) which is higher than Zn2SnO4 nanoparticle (η = 2.52%) based perovskite solar cells. This improvement is achieved due to high porosity of Zn2SnO4 nanofibers and high crystallinity of the nanofibers synthesized at 700 °C. These results are remarkably higher than reported perovskite solar cells based on such type of ternary metal oxide ETLs.

  8. Graphitized-Carbon-Nanofiber Paper-Enzyme Electrode Fabrication Through Non-Covalent Modification for Enzyme Biofuel Cell Application.

    PubMed

    Fapyane, Deby; Lee, Soo-Jin; Kang, Seung-Hwan; Ahn, Jou-Hyeon; Chang, In Seop

    2015-01-01

    Carbon nanofibers are an emerging smart material that are promising for use as a biosensor and a biofuel cell transducer material due to their morphological and electrochemical characteristics. In particular, graphitized carbon nanofibers possess unique structures of graphite-like edges within their high surface area that provide a large active site for enzyme attachment. For a specific application such as a biofuel cell, which requires highly stable electrical communication and electricity generation, non-covalent enzyme immobilization using bifunctional molecule is suggested as an appropriate approach because it does not change the carbon hybridization from sp2 to sp3 as covalent immobilization by acid treatment does. Graphitized carbon-nanofiber paper (GCNFp) electrode were fabricated through dispersion-filtration method in which glucose oxidase as model enzyme were immobilized by a bifunctional molecule that forms π-π stacking of the pyrene moiety with the nanofiber wall coupled by a reactive end-amine reaction. This system provides a practical enzyme-electrode hybrid that facilitates comparatively faster enzyme-electrode electrical communication than other system using similar material, as calculated from the heterogeneous electron-transfer rate constant (K(s)) which was 5.45 s(-1). PMID:26301307

  9. LiFePO4 - 3D carbon nanofiber composites as cathode materials for Li-ions batteries

    NASA Astrophysics Data System (ADS)

    Dimesso, L.; Spanheimer, C.; Jaegermann, W.; Zhang, Y.; Yarin, A. L.

    2012-03-01

    The characterization of carbon nanofiber 3D nonwovens, prepared by electrospinning process, coated with olivine structured lithium iron phosphate is reported. The LiFePO4 as cathode material for lithium ion batteries was prepared by a Pechini-assisted reversed polyol process. The coating has been successfully performed on carbon nanofiber 3D nonwovens by soaking in aqueous solution containing lithium, iron salts and phosphates at 70 °C for 2-4 h. After drying-out, the composites were annealed at 600 °C for 5 h under nitrogen. The surface investigation of the prepared composites showed a uniform coating of the carbon nonwoven nanofibers as well as the formation of cauliflower-like crystalline structures which are uniformly distributed all over the surface area of the carbon nanofibers. The electrochemical measurements on the composites showed good performances delivering a discharge specific capacity of 156 mAhg- 1 at a discharging rate of C/25 and 152 mAhg- 1 at a discharging rate of C/10 at room temperature.

  10. Sorption kinetics of heavy oil into porous carbons.

    PubMed

    Nishi, Yoko; Iwashita, Norio; Sawada, Yoshihiro; Inagaki, Michio

    2002-12-01

    Sorption kinetics of heavy oil into porous carbons was evaluated by a concept of liquid sorption coefficient obtained from the weight increase of heavy oil with sorption time, which was measured by a wicking test. Exfoliated graphite, carbonized fir fibers and carbon fiber felts were used as porous materials. It was found that the liquid sorption coefficient of fibrous carbons was twice larger than that of exfoliated graphite. Such a difference in the liquid sorption coefficient between the exfoliated graphite and two fibrous carbons was caused by a difference in effective sorption porosity and tortuosity between them. For the exfoliated graphite and carbonized fir fibers, the liquid sorption coefficient and the effective sorption porosity were strongly dependent on their density. The maximum values of both liquid sorption coefficient and effective sorption porosity of the exfoliated graphite were shown at the bulk density around 16 kg/m3. The liquid sorption coefficient of the carbonized fir fibers increased with increasing the density in the range from 6 to 30 kg/m3. When the carbonized fir fibers were densified above 30 kg/m3, the sorption rate was saturated. On the other hand, the sorption kinetics into the carbon fiber felt was almost independent of the bulk density, because the density of the carbon fiber felt is not effective for the pore structure. The effect of bulk density on the sorption kinetics could be supported from an analysis of pore structure of the porous carbons with different densities, which was measured by mercury porosimeter. PMID:12448551

  11. Carbon nanotube-templated polyaniline nanofibers: synthesis, flash welding and ultrafiltration membranes

    NASA Astrophysics Data System (ADS)

    Liao, Yaozu; Yu, Deng-Guang; Wang, Xia; Chain, Wei; Li, Xin-Gui; Hoek, Eric M. V.; Kaner, Richard B.

    2013-04-01

    Electro-active switchable ultrafiltration membranes are of great interest due to the possibility of external control over permeability, selectivity, anti-fouling and cleaning. Here, we report on hybrid single-walled carbon nanotube (SWCNT)-polyaniline (PANi) nanofibers synthesized by in situ polymerization of aniline in the presence of oxidized SWCNTs. The composite nanofibers exhibit unique morphology of core-shell (SWCNT-PANi) structures with average total diameters of 60 nm with 10 to 30 nm thick PANi coatings. The composite nanofibers are easily dispersed in polar aprotic solvents and cast into asymmetric membranes via a nonsolvent induced phase separation. The hybrid SWCNT-PANi membranes are electrically conductive at neutral pH and exhibit ultrafiltration-like permeability and selectivity when filtering aqueous suspensions of 6 nm diameter bovine serum albumin and 48 nm diameter silica particles. A novel flash welding technique is utilized to tune the morphology, porosity, conductivity, permeability and nanoparticle rejection of the SWCNT-PANi composite ultrafiltration membranes. Upon flash welding, both conductivity and pure water permeability of the membranes improves by nearly a factor of 10, while maintaining silica nanoparticle rejection levels above 90%. Flash welding of SWCNT-PANi composite membranes holds promise for formation of electrochemically tunable membranes.Electro-active switchable ultrafiltration membranes are of great interest due to the possibility of external control over permeability, selectivity, anti-fouling and cleaning. Here, we report on hybrid single-walled carbon nanotube (SWCNT)-polyaniline (PANi) nanofibers synthesized by in situ polymerization of aniline in the presence of oxidized SWCNTs. The composite nanofibers exhibit unique morphology of core-shell (SWCNT-PANi) structures with average total diameters of 60 nm with 10 to 30 nm thick PANi coatings. The composite nanofibers are easily dispersed in polar aprotic solvents and

  12. Mass Production of Carbon Nanofibers Using Microwave Technology.

    PubMed

    Mubarak, N M; Abdullah, E C; Sahu, J N; Jayakumar, N S; Ganesan, P

    2015-12-01

    Carbon nanotubes (CNFs) were produced by gas phase single stage microwave assisted chemical vapour deposition (MA-CVD) using ferrocene as a catalyst and acetylene (C2H2) and hydrogen (H2) as precursor gases. The effect of the process parameters such as microwave power, radiation time, and gas ratio of C2H2/H2 was investigated. The CNFs were characterized using scanning and transmission electron microscopy (TEM), and by thermogravimetric analysis (TGA). Results reveal that the optimized conditions for CNF production were 1000 W reaction power, 35 min radiation time, and 0.8 gas ratio of C2H2/H2. TEM analyses revealed that the uniformly dispersed CNFs diameters ranging from 115-131 nm. The TGA analysis showed that the purity of CNF produced was 93%. PMID:26682380

  13. Electrospun composite nanofibers of poly vinyl pyrrolidone and zinc oxide nanoparticles modified carbon paste electrode for electrochemical detection of curcumin.

    PubMed

    Afzali, Moslem; Mostafavi, Ali; Shamspur, Tayebeh

    2016-11-01

    A simple and novel ferrocene-nanofiber carbon paste electrode was developed to determine curcumin in a phosphate buffer solution at pH=8. ZnO nanoparticles were produced via a sonochemical process and composite nanofibers of PVP/ZnO were prepared by electrospinning. The characterization was performed by SEM, XRD and IR. The results suggest that the electrospun composite nanofibers having a large surface area promote electron transfer for the oxidation of curcumin and hence the FCNFCPE exhibits high electrocatalytic activity and performs well in regard to the oxidation of curcumin. The proposed method was successfully applied for measurement of curcumin in urine and turmeric as real samples. PMID:27524081

  14. Molten carbonate fuel cell (MCFC) porous electrode and kinetic studies

    SciTech Connect

    Selman, J.R. )

    1992-10-01

    This report sumarizes a research project undertaken to improve the performance and understand the limitations of porous electrodes for molten carbonate fuel cells (MCFCs). Using a novel MCFC rotating-disk'' electrode, the electrode kinetic and mass transfer properties of commonly used electrode materials were determined, and a practical performance model for MCFC electrodes was developed. The report also outlines a general strategy for designing a high-performance MCFC electrode, assesses the current understanding of porous electrode operation, and discusses some of the unresolved questions of the field. An appendix gives a complete list of the many theses, journal articles, and symposium contributions based on this research.

  15. In situ Polymerization of Multi-Walled Carbon Nanotube/Nylon-6 Nanocomposites and Their Electrospun Nanofibers.

    PubMed

    Saeed, Khalid; Park, Soo-Young; Haider, Sajjad; Baek, Jong-Beom

    2009-01-01

    Multiwalled carbon nanotube/nylon-6 nanocomposites (MWNT/nylon-6) were prepared by in situ polymerization, whereby functionalized MWNTs (F-MWNTs) and pristine MWNTs (P-MWNTs) were used as reinforcing materials. The F-MWNTs were functionalized by Friedel-Crafts acylation, which introduced aromatic amine (COC(6)H(4)-NH(2)) groups onto the side wall. Scanning electron microscopy (SEM) images obtained from the fractured surfaces of the nanocomposites showed that the F-MWNTs in the nylon-6 matrix were well dispersed as compared to those of the P-MWNTs. Both nanocomposites could be electrospun into nanofibers in which the MWNTs were embedded and oriented along the nanofiber axis, as confirmed by transmission electron microscopy. The specific strength and modulus of the MWNTs-reinforced nanofibers increased as compared to those of the neat nylon-6 nanofibers. The crystal structure of the nylon-6 in the MWNT/nylon-6 nanofibers was mostly gamma-phase, although that of the MWNT/nylon-6 films, which were prepared by hot-pressing the pellets between two aluminum plates and then quenching them in icy water, was mostly alpha-phase, indicating that the shear force during electrospinning might favor the gamma-phase, similarly to the conventional fiber spinning. PMID:20596470

  16. Preparation of poly(L-lactic acid) nanofiber scaffolds with a rough surface by phase inversion using supercritical carbon dioxide.

    PubMed

    Yang, Ding-Zhu; Chen, Ai-Zheng; Wang, Shi-Bin; Li, Yi; Tang, Xiao-Lin; Wu, Yong-Jing

    2015-06-01

    Phase inversion using supercritical carbon dioxide (SC-CO2) has been widely used in the development of tissue engineering scaffolds, and particular attention has been given to obtaining desired morphology without additional post-treatments. However, the main challenge of this technique is the difficulty in generating a three-dimensional (3D) nanofiber structure with a rough surface in one step. Here, a poly(L-lactic acid) (PLLA) 3D nanofiber scaffold with a rough surface is obtained via phase inversion using SC-CO2 by carefully choosing fabrication conditions and porogens. It is found that this method can effectively modulate the structure morphology, promote the crystallization process of semicrystalline polymer, and induce the formation of rough structures on the surface of nanofibers. Meanwhile, the porogen of ammonium bicarbonate (AB) can produce a 3D structure with large pores, and porogen of menthol can improve the interconnectivity between the micropores of nanofibers. A significant increase in the fiber diameter is observed as the menthol content increases. Furthermore, the menthol may affect the mutual transition between the α' and α crystals of PLLA during the phase separation process. In addition, the results of protein adsorption, cell adhesion, and proliferation assays indicate that cells tend to have higher viability on the nanofiber scaffold. This process combines the characteristic properties of SC-CO2 and the solubility of menthol to tailor the morphology of polymeric scaffolds, which may have potential applications in tissue engineering. PMID:26107415

  17. Influence of PVP template on the formation of porous TiO2 nanofibers by electrospinning technique for dye-sensitized solar cell

    NASA Astrophysics Data System (ADS)

    Elayappan, Vijayakumar; Panneerselvam, Pratheep; Nemala, Sivasankar; Nallathambi, Karthick S.; Angaiah, Subramania

    2015-09-01

    The porous TiO2 nanofibers were prepared by electrospinning technique using polyvinylpyrrolidone (PVP) as template as well as pore-forming agent at the calcination temperature of 475 °C for 5 h. The influence of various concentrations of PVP (5, 8 and 10 wt%) on the surface area and porosity of the prepared TiO2 nanofibers (NFs) were studied by using BET-specific surface area analyzer. The TiO2 NFs obtained by using 5 wt% of PVP had higher surface area and porosity than those obtained by using 8 and 10 wt% of PVP. The prepared electrospun TiO2 NFs were characterized by using TG analysis, X-ray diffraction, FTIR, FE-SEM and TEM studies. Finally, dye-sensitized solar cells were assembled using the prepared TiO2 NFs as the photoanode, Pt as the cathode and 0.5 M 1-butyl-3-methylimidazolium iodide, 0.5 M LiI, 0.05 M I2, 0.5 M 4-tertbutylpyridine in acetonitrile as an electrolyte. Among the three photoanodes, the cell assembled using porous TiO2 NFs obtained by using 5 wt% of PVP showed higher power conversion efficiency (PCE) of 4.81 % than those obtained by using 8 and 10 wt% of PVP, which showed the lower PCE of 4.13 and 3.42 %, respectively.

  18. Inhalation Exposure to Carbon Nanotubes (CNT) and Carbon Nanofibers (CNF): Methodology and Dosimetry.

    PubMed

    Oberdörster, Günter; Castranova, Vincent; Asgharian, Bahman; Sayre, Phil

    2015-01-01

    Carbon nanotubes (CNT) and nanofibers (CNF) are used increasingly in a broad array of commercial products. Given current understandings, the most significant life-cycle exposures to CNT/CNF occur from inhalation when they become airborne at different stages of their life cycle, including workplace, use, and disposal. Increasing awareness of the importance of physicochemical properties as determinants of toxicity of CNT/CNF and existing difficulties in interpreting results of mostly acute rodent inhalation studies to date necessitate a reexamination of standardized inhalation testing guidelines. The current literature on pulmonary exposure to CNT/CNF and associated effects is summarized; recommendations and conclusions are provided that address test guideline modifications for rodent inhalation studies that will improve dosimetric extrapolation modeling for hazard and risk characterization based on the analysis of exposure-dose-response relationships. Several physicochemical parameters for CNT/CNF, including shape, state of agglomeration/aggregation, surface properties, impurities, and density, influence toxicity. This requires an evaluation of the correlation between structure and pulmonary responses. Inhalation, using whole-body exposures of rodents, is recommended for acute to chronic pulmonary exposure studies. Dry powder generator methods for producing CNT/CNF aerosols are preferred, and specific instrumentation to measure mass, particle size and number distribution, and morphology in the exposure chambers are identified. Methods are discussed for establishing experimental exposure concentrations that correlate with realistic human exposures, such that unrealistically high experimental concentrations need to be identified that induce effects under mechanisms that are not relevant for workplace exposures. Recommendations for anchoring data to results seen for positive and negative benchmark materials are included, as well as periods for postexposure observation

  19. INHALATION EXPOSURE TO CARBON NANOTUBES (CNT) AND CARBON NANOFIBERS (CNF): METHODOLOGY AND DOSIMETRY

    PubMed Central

    Oberdörster, Günter; Castranova, Vincent; Asgharian, Bahman; Sayre, Phil

    2015-01-01

    Carbon nanotubes (CNT) and nanofibers (CNF) are used increasingly in a broad array of commercial products. Given current understandings, the most significant life-cycle exposures to CNT/CNF occur from inhalation when they become airborne at different stages of their life cycle, including workplace, use, and disposal. Increasing awareness of the importance of physicochemical properties as determinants of toxicity of CNT/CNF and existing difficulties in interpreting results of mostly acute rodent inhalation studies to date necessitate a reexamination of standardized inhalation testing guidelines. The current literature on pulmonary exposure to CNT/CNF and associated effects is summarized; recommendations and conclusions are provided that address test guideline modifications for rodent inhalation studies that will improve dosimetric extrapolation modeling for hazard and risk characterization based on the analysis of exposure-dose-response relationships. Several physicochemical parameters for CNT/CNF, including shape, state of agglomeration/aggregation, surface properties, impurities, and density, influence toxicity. This requires an evaluation of the correlation between structure and pulmonary responses. Inhalation, using whole-body exposures of rodents, is recommended for acute to chronic pulmonary exposure studies. Dry powder generator methods for producing CNT/CNF aerosols are preferred, and specific instrumentation to measure mass, particle size and number distribution, and morphology in the exposure chambers are identified. Methods are discussed for establishing experimental exposure concentrations that correlate with realistic human exposures, such that unrealistically high experimental concentrations need to be identified that induce effects under mechanisms that are not relevant for workplace exposures. Recommendations for anchoring data to results seen for positive and negative benchmark materials are included, as well as periods for postexposure observation

  20. Induced Potential in Porous Carbon Films through Water Vapor Absorption.

    PubMed

    Liu, Kang; Yang, Peihua; Li, Song; Li, Jia; Ding, Tianpeng; Xue, Guobin; Chen, Qian; Feng, Guang; Zhou, Jun

    2016-07-01

    Sustainable electrical potential of tens of millivolts can be induced by water vapor adsorption on a piece of porous carbon film that has two sides with different functional group contents. Integrated experiments, and Monte Carlo and ab initio molecular dynamics simulations reveal that the induced potential originates from the nonhomogeneous distribution of functional groups along the film, especially carboxy groups. Sufficient adsorbed water molecules in porous carbon facilitate the release of protons from the carboxy groups, resulting in a potential drop across the carbon film because of the concentration difference of the released free protons on the two sides. The potential utilization of such a phenomenon is also demonstrated by a self-powered humidity sensor. PMID:27159427

  1. Synthesis and characterization of magnetically active carbon nanofiber/iron oxide composites with hierarchical pore structures

    NASA Astrophysics Data System (ADS)

    Panels, Jeanne E.; Lee, Jinwoo; Park, Kang Yeol; Kang, Seung Yeon; Marquez, Manuel; Wiesner, Ulrich; Lak Joo, Yong

    2008-11-01

    Polyacrylonitrile (PAN) solution containing the iron oxide precursor iron (III) acetylacetonate (AAI) was electrospun and thermally treated to produce electrically conducting, magnetic carbon nanofiber mats with hierarchical pore structures. The morphology and material properties of the resulting multifunctional nanofiber mats including the surface area and the electric and magnetic properties were examined using various characterization techniques. Scanning electron microscopy images show that uniform fibers were produced with a fiber diameter of ~600 nm, and this uniform fiber morphology is maintained after graphitization with a fiber diameter of ~330 nm. X-ray diffraction (XRD) and Raman studies reveal that both graphite and Fe3O4 crystals are formed after thermal treatment, and graphitization can be enhanced by the presence of iron. A combination of XRD and transmission electron microscopy experiments reveals the formation of pores with graphitic nanoparticles in the walls as well as the formation of magnetite nanoparticles distributed throughout the fibers. Physisorption experiments show that the multifunctional fiber mats exhibit a high surface area (200-400 m2 g-1) and their pore size is dependent on the amount of iron added and graphitization conditions. Finally, we have demonstrated that the fibers are electrically conducting as well as magnetically active.

  2. Direct electrochemistry of glucose oxidase on novel free-standing nitrogen-doped carbon nanospheres@carbon nanofibers composite film.

    PubMed

    Zhang, Xueping; Liu, Dong; Li, Libo; You, Tianyan

    2015-01-01

    We have proposed a novel free-standing nitrogen-doped carbon nanospheres@carbon nanofibers (NCNSs@CNFs) composite film with high processability for the investigation of the direct electron transfer (DET) of glucose oxidase (GOx) and the DET-based glucose biosensing. The composites were simply prepared by controlled thermal treatment of electrospun polypyrrole nanospheres doped polyacrylonitrile nanofibers (PPyNSs@PAN NFs). Without any pretreatment, the as-prepared material can directly serve as a platform for GOx immobilization. The cyclic voltammetry of immobilized GOx showed a pair of well-defined redox peaks in O2-free solution, indicating the DET of GOx. With the addition of glucose, the anodic peak current increased, while the cathodic peak current decreased, which demonstrated the DET-based bioelectrocatalysis. The detection of glucose based on the DET of GOx was achieved, which displayed high sensitivity, stability and selectivity, with a low detection limit of 2 μM and wide linear range of 12-1000 μM. These results demonstrate that the as-obtained NCNSs@CNFs can serve as an ideal platform for the construction of the third-generation glucose biosensor. PMID:25943704

  3. Direct Electrochemistry of Glucose Oxidase on Novel Free-Standing Nitrogen-Doped Carbon Nanospheres@Carbon Nanofibers Composite Film

    NASA Astrophysics Data System (ADS)

    Zhang, Xueping; Liu, Dong; Li, Libo; You, Tianyan

    2015-05-01

    We have proposed a novel free-standing nitrogen-doped carbon nanospheres@carbon nanofibers (NCNSs@CNFs) composite film with high processability for the investigation of the direct electron transfer (DET) of glucose oxidase (GOx) and the DET-based glucose biosensing. The composites were simply prepared by controlled thermal treatment of electrospun polypyrrole nanospheres doped polyacrylonitrile nanofibers (PPyNSs@PAN NFs). Without any pretreatment, the as-prepared material can directly serve as a platform for GOx immobilization. The cyclic voltammetry of immobilized GOx showed a pair of well-defined redox peaks in O2-free solution, indicating the DET of GOx. With the addition of glucose, the anodic peak current increased, while the cathodic peak current decreased, which demonstrated the DET-based bioelectrocatalysis. The detection of glucose based on the DET of GOx was achieved, which displayed high sensitivity, stability and selectivity, with a low detection limit of 2 μM and wide linear range of 12-1000 μM. These results demonstrate that the as-obtained NCNSs@CNFs can serve as an ideal platform for the construction of the third-generation glucose biosensor.

  4. Direct Electrochemistry of Glucose Oxidase on Novel Free-Standing Nitrogen-Doped Carbon Nanospheres@Carbon Nanofibers Composite Film

    PubMed Central

    Zhang, Xueping; Liu, Dong; Li, Libo; You, Tianyan

    2015-01-01

    We have proposed a novel free-standing nitrogen-doped carbon nanospheres@carbon nanofibers (NCNSs@CNFs) composite film with high processability for the investigation of the direct electron transfer (DET) of glucose oxidase (GOx) and the DET-based glucose biosensing. The composites were simply prepared by controlled thermal treatment of electrospun polypyrrole nanospheres doped polyacrylonitrile nanofibers (PPyNSs@PAN NFs). Without any pretreatment, the as-prepared material can directly serve as a platform for GOx immobilization. The cyclic voltammetry of immobilized GOx showed a pair of well-defined redox peaks in O2-free solution, indicating the DET of GOx. With the addition of glucose, the anodic peak current increased, while the cathodic peak current decreased, which demonstrated the DET-based bioelectrocatalysis. The detection of glucose based on the DET of GOx was achieved, which displayed high sensitivity, stability and selectivity, with a low detection limit of 2 μM and wide linear range of 12–1000 μM. These results demonstrate that the as-obtained NCNSs@CNFs can serve as an ideal platform for the construction of the third-generation glucose biosensor. PMID:25943704

  5. Supported porous carbon and carbon-CNT nanocomposites for supercapacitor applications

    NASA Astrophysics Data System (ADS)

    Schopf, Dimitri; Es-Souni, Mohammed

    2016-03-01

    Supported porous carbon and porous carbon-MWCNT-nanocomposite films are produced by pyrolysis of porous polyvinylidene fluoride (PVDF) or porous PVDF-MWCNT-nanocomposite films on thermally resistant substrates. All films are characterized by SEM, RAMAN and XRD. The application of these films as supercapacitors is explored with outstanding supercapacitance values ranging from 80 to 120 F g-1 (up to 70 mF cm-2) in a three-electrode set-up in 1 M KOH, depending on microstructure. Additionally, the implementation of porous nanocarbon-MWCNT-nanocomposite films as electrodes in a symmetrical supercapacitor device is investigated. In all cases, long-term charge-discharge stability is demonstrated.

  6. Characterization of porous carbon fibers and related materials

    SciTech Connect

    Fuller, E.L. Jr.

    1996-07-15

    This program was geared to support the Fossil Energy Material Sciences Program with respect to several areas of interest in efficient production and utilization of energy. Carbon molecular sieves have great potential for economically purifying gases; i.e. removal of carbon dioxide from natural gas without having to resort to cryogenic techniques. Microporous carbons can be tailored to serve as adsorbents for natural gas in on-board storage in automotive applications, avoiding high pressures and heavy storage tanks. This program is a laboratory study to evaluate production methodologies and activation processes to produce porous carbons for specific applications. The Carbon Materials Technology Group of Oak Ridge National Laboratory (ORNL) is engaged in developmental programs to produce activated carbon fibers (ACF) for applications in fixed beds and/or flowing reactors engineering applications.

  7. Lithium intercalation in porous carbon electrodes

    SciTech Connect

    Tran, T.D.; Feikert, J.; Pekala, R.W.

    1995-04-01

    Carbons derived from the phase separation of polyacrylonitrile/solvent mixtures were investigated as lithium intercalation anodes for rechargeable lithium-ion batteries. The carbon electrodes have a bulk density of 0.35-0.5 g/cm{sup 3}, relatively low surface areas (< 10 m{sup 2}/g), and micron-size cells. Pyrolysis temperature influences the reversible lithium intercalation and the irreversible capacity (associated with the formation of the passivating layer). Carbon electrodes pyrolyzed at 600{degrees}C have first-cycle capacity as high as 550 mAh/g as well as large irreversible capacity, 440 mAh/g. Electrodes prepared at 1050{degrees}C have reversible capacities around 270 mAh/g with relatively lower capacity losses (120 mAh/g). Doping the organic precursors with phosphoric acid, prior to pyrolysis at 1050{degrees}C, leads to carbon electrodes with reversible capacities as high as 450 mAh/g. The capacity of doped carbon increased with increasing phosphorus concentration in the samples. The doped carbon anodes exhibited good cycleability and excellent coulombic efficiency. The electrochemical performance is related to morphology, chemical composition, and local structural order.

  8. Spherical and rodlike inorganic nanoparticle regulated the orientation of carbon nanotubes in polymer nanofibers

    NASA Astrophysics Data System (ADS)

    Jiang, Linbin; Tu, Hu; Lu, Yuan; Wu, Yang; Tian, Jing; Shi, Xiaowen; Wang, Qun; Zhan, Yingfei; Huang, Zuqiang; Deng, Hongbing

    2016-04-01

    PVA nanofibers containing carboxylic-modified MWCNTs were fabricated via electrospinning of PVA/MWCNTs mixed solution. The alignment of MWCNTs in PVA nanofibers was studied using transmission electron microscope and scanning electron microscope. In addition, the orientation of MWCNTs in PVA nanofibers was further investigated in the presence of rod-like nanoparticle rectorite (REC) and of spherical nanoparticle titanium dioxide (TiO2). The images demonstrated the embedment of MWCNTs in the nanofibers and the alignment of MWCNTs along the fiber axis. Moreover, the addition of REC and TiO2 improved the alignment of MWCNTs in PVA nanofibers.

  9. Graphitic Carbon-Coated FeSe2 Hollow Nanosphere-Decorated Reduced Graphene Oxide Hybrid Nanofibers as an Efficient Anode Material for Sodium Ion Batteries

    NASA Astrophysics Data System (ADS)

    Cho, Jung Sang; Lee, Jung-Kul; Kang, Yun Chan

    2016-04-01

    A novel one-dimensional nanohybrid comprised of conductive graphitic carbon (GC)-coated hollow FeSe2 nanospheres decorating reduced graphene oxide (rGO) nanofiber (hollow nanosphere FeSe2@GC–rGO) was designed as an efficient anode material for sodium ion batteries and synthesized by introducing the nanoscale Kirkendall effect into the electrospinning method. The electrospun nanofibers transformed into hollow nanosphere FeSe2@GC–rGO hybrid nanofibers through a Fe@GC–rGO intermediate. The discharge capacities of the bare FeSe2 nanofibers, nanorod FeSe2–rGO–amorphous carbon (AC) hybrid nanofibers, and hollow nanosphere FeSe2@GC–rGO hyrbid nanofibers at a current density of 1 A g‑1 for the 150th cycle were 63, 302, and 412 mA h g‑1, respectively, and their corresponding capacity retentions measured from the 2nd cycle were 11, 73, and 82%, respectively. The hollow nanosphere FeSe2@GC–rGO hybrid nanofibers delivered a high discharge capacity of 352 mA h g‑1 even at an extremely high current density of 10 A g‑1. The enhanced electrochemical properties of the hollow nanosphere FeSe2@GC–rGO composite nanofibers arose from the synergetic effects of the FeSe2 hollow morphology and highly conductive rGO matrix.

  10. Graphitic Carbon-Coated FeSe2 Hollow Nanosphere-Decorated Reduced Graphene Oxide Hybrid Nanofibers as an Efficient Anode Material for Sodium Ion Batteries

    PubMed Central

    Cho, Jung Sang; Lee, Jung-Kul; Kang, Yun Chan

    2016-01-01

    A novel one-dimensional nanohybrid comprised of conductive graphitic carbon (GC)-coated hollow FeSe2 nanospheres decorating reduced graphene oxide (rGO) nanofiber (hollow nanosphere FeSe2@GC–rGO) was designed as an efficient anode material for sodium ion batteries and synthesized by introducing the nanoscale Kirkendall effect into the electrospinning method. The electrospun nanofibers transformed into hollow nanosphere FeSe2@GC–rGO hybrid nanofibers through a Fe@GC–rGO intermediate. The discharge capacities of the bare FeSe2 nanofibers, nanorod FeSe2–rGO–amorphous carbon (AC) hybrid nanofibers, and hollow nanosphere FeSe2@GC–rGO hyrbid nanofibers at a current density of 1 A g−1 for the 150th cycle were 63, 302, and 412 mA h g−1, respectively, and their corresponding capacity retentions measured from the 2nd cycle were 11, 73, and 82%, respectively. The hollow nanosphere FeSe2@GC–rGO hybrid nanofibers delivered a high discharge capacity of 352 mA h g−1 even at an extremely high current density of 10 A g−1. The enhanced electrochemical properties of the hollow nanosphere FeSe2@GC–rGO composite nanofibers arose from the synergetic effects of the FeSe2 hollow morphology and highly conductive rGO matrix. PMID:27033096

  11. Chemoselective hydrogenation of functionalized nitroarenes and imines by using carbon nanofiber-supported iridium nanoparticles.

    PubMed

    Motoyama, Yukihiro; Taguchi, Masahiro; Desmira, Nelfa; Yoon, Seong-Ho; Mochida, Isao; Nagashima, Hideo

    2014-01-01

    The reaction of three types of carbon nanofibers (CNFs; platelet: CNF-P, tubular: CNF-T, herringbone: CNF-H) with Ir4(CO)12 in mesitylene at 165 °C provided the corresponding CNF-supported iridium nanoparticles, Ir/CNFs (Ir content=2.3-2.6 wt.%). Transmission electron microscopy (TEM) studies of these Ir/CNF samples revealed that size-controlled Ir nanoparticles (average particle size of 1.1-1.5 nm) existed on the CNFs. Among the three Ir/CNF samples, Ir/CNF-T showed an excellent catalytic activity and chemoselectivity towards hydrogenation of functionalized nitroarenes and imines; the corresponding aniline derivatives were obtained with high turnover numbers at ambient temperature under 10 tm of H2 , and the catalyst is reusable. Ir/CNF-T was also effective for the reductive N-alkylation of anilines with carbonyl compounds. PMID:24347068

  12. Electrosorption of ions from aqueous solutions with carbon nanotubes and nanofibers composite film electrodes

    SciTech Connect

    Wang, X. Z.; Li, M. G.; Chen, Y. W.; Cheng, R. M.; Huang, S. M.; Pan, L. K.; Sun, Z.

    2006-07-31

    Electrosorption of ions from aqueous solutions with carbon nanotubes and nanofibers (CNTs-CNFs) composite film electrodes has been demonstrated. The large area CNTs-CNFs film was directly grown on Ni plate by low pressure and low temperature thermal chemical vapor deposition. The CNTs-CNFs electrodes have great advantages such as low cost, easy operation, long-term reproducibility, and integrity of monolithic CNTs-CNFs film and current collector. Batch-mode experiments at low voltage (0.4-2 V) were conducted in a continuously recycling system to investigate the electrosorption process. Purification of water with good reproducibility was achieved because of optimal pore size distribution of CNTs-CNFs composite films.

  13. Fabrication and Properties of Ethylene Vinyl Acetate-Carbon Nanofiber Nanocomposites

    PubMed Central

    2008-01-01

    Carbon nanofiber (CNF) is one of the stiffest materials produced commercially, having excellent mechanical, electrical, and thermal properties. The reinforcement of rubbery matrices by CNFs was studied in the case of ethylene vinyl acetate (EVA). The tensile strength was greatly (61%) increased, even for very low fiber content (i.e., 1.0 wt.%). The surface modification of the fiber by high energy electron beam and gamma irradiation led to better dispersion in the rubber matrix. This in turn gave rise to further improvements in mechanical and dynamic mechanical properties of EVA. The thermal conductivity also exhibited improvements from that of the neat elastomer, although thermal stability of the nanocomposites was not significantly altered by the functionalization of CNFs. Various results were well supported by the morphological analysis of the nanocomposites. PMID:20596388

  14. Carbon Nanofibers Modified Graphite Felt for High Performance Anode in High Substrate Concentration Microbial Fuel Cells

    PubMed Central

    Shen, Youliang; Zhou, Yan; Chen, Shuiliang; Yang, Fangfang; Zheng, Suqi; Hou, Haoqing

    2014-01-01

    Carbon nanofibers modified graphite fibers (CNFs/GF) composite electrode was prepared for anode in high substrate concentration microbial fuel cells. Electrochemical tests showed that the CNFs/GF anode generated a peak current density of 2.42 mA cm−2 at a low acetate concentration of 20 mM, which was 54% higher than that from bare GF. Increase of the acetate concentration to 80 mM, in which the peak current density of the CNFs/GF anode greatly increased and was up to 3.57 mA cm−2, was seven times as that of GF anode. Morphology characterization revealed that the biofilms in the CNFs/GF anode were much denser than those in the bare GF. This result revealed that the nanostructure in the anode not only enhanced current generation but also could tolerate high substrate concentration. PMID:24883348

  15. Electrorheological fluid effect of polymer coated carbon nanofibers and/or fullerenes in liquid crystals

    NASA Astrophysics Data System (ADS)

    French, Steven S.

    An ER fluid is a 'smart' visco-elastic material, with flow properties influenced by external electric fields, whereby its viscosity increases within the field and returns to its inherent viscosity without the field present. This unique behavior opens many possibilities for new technologies. The optimization of ER fluid performance depends on the chemical and structural compositions of the particles in suspension and the suspension itself. Recent inclusion of nano-particles within ER fluids has shown a relationship to favorable ER trends. Therefore, this research involved nano-laden ER fluid samples of fullerenes (C60) and/or polymer coated carbon nano-fibers as the dispersed phases. These nano-particles were dispersed within either silicone oil, polyethylene oxide/water or three different liquid crystal types.

  16. A Glucose Biosensor Using CMOS Potentiostat and Vertically Aligned Carbon Nanofibers.

    PubMed

    Al Mamun, Khandaker A; Islam, Syed K; Hensley, Dale K; McFarlane, Nicole

    2016-08-01

    This paper reports a linear, low power, and compact CMOS based potentiostat for vertically aligned carbon nanofibers (VACNF) based amperometric glucose sensors. The CMOS based potentiostat consists of a single-ended potential control unit, a low noise common gate difference-differential pair transimpedance amplifier and a low power VCO. The potentiostat current measuring unit can detect electrochemical current ranging from 500 nA to 7 [Formula: see text] from the VACNF working electrodes with high degree of linearity. This current corresponds to a range of glucose, which depends on the fiber forest density. The potentiostat consumes 71.7 [Formula: see text] of power from a 1.8 V supply and occupies 0.017 [Formula: see text] of chip area realized in a 0.18 [Formula: see text] standard CMOS process. PMID:27337723

  17. Carbon nanofiber supported bimetallic PdAu nanoparticles for formic acid electrooxidation

    NASA Astrophysics Data System (ADS)

    Qin, Yuan-Hang; Jiang, Yue; Niu, Dong-Fang; Zhang, Xin-Sheng; Zhou, Xing-Gui; Niu, Li; Yuan, Wei-Kang

    2012-10-01

    Carbon nanofiber (CNF) supported PdAu nanoparticles are synthesized with sodium citrate as the stabilizing agent and sodium borohydride as the reducing agent. High resolution transmission electron microscopy (HRTEM) characterization indicates that the synthesized PdAu particles are well dispersed on the CNF surface and X-ray diffraction (XRD) characterization indicates that the alloying degree of the synthesized PdAu nanoparticles can be improved by adding tetrahydrofuran to the synthesis solution. The results of electrochemical characterization indicate that the addition of Au can promote the electrocatalytic activity of Pd/C catalyst for formic acid oxidation and the CNF supported high-alloying PdAu catalyst possesses better electrocatalytic activity and stability for formic acid oxidation than either the CNF supported low-alloying PdAu catalyst or the CNF supported Pd catalyst.

  18. Synthesis of highly dispersed and active palladium/carbon nanofiber catalyst for formic acid electrooxidation

    NASA Astrophysics Data System (ADS)

    Qin, Yuan-Hang; Yue-Jiang; Yang, Hou-Hua; Zhang, Xin-Sheng; Zhou, Xing-Gui; Niu, Li; Yuan, Wei-Kang

    2011-05-01

    Highly dispersed and active palladium/carbon nanofiber (Pd/CNF) catalyst is synthesized by NaBH4 reduction with trisodium citrate as the stabilizing agent. The obtained Pd/CNF catalyst is characterized by high resolution transmission electron microscopy (HRTEM) and X-ray diffraction (XRD). The results show that the Pd nanoparticles with an average particle size of ca. 3.8 nm are highly dispersed on the CNF support even with a small ratio of citrate to Pd precursor, which is believed to be due to the pH adjustment of citrate stabilized colloidal Pd nanoparticles. The cyclic voltammetry and chronoamperometry techniques show that the obtained Pd/CNF catalyst exhibits good catalytic activity and stability for the electrooxidation of formic acid.

  19. Carbon nanofiber aerogels for emergent cleanup of oil spillage and chemical leakage under harsh conditions

    PubMed Central

    Wu, Zhen-Yu; Li, Chao; Liang, Hai-Wei; Zhang, Yu-Ning; Wang, Xin; Chen, Jia-Fu; Yu, Shu-Hong

    2014-01-01

    To address oil spillage and chemical leakage accidents, the development of efficient sorbent materials is of global importance for environment and water source protection. Here we report on a new type of carbon nanofiber (CNF) aerogels as efficient sorbents for oil uptake with high sorption capacity and excellent recyclability. Importantly, the oil uptake ability of the CNF aerogels can be maintained over a wide temperature range, from liquid nitrogen temperature up to ca. 400°C, making them suitable for oil cleanup under harsh conditions. The outstanding sorption performance of CNF aerogels is associated with their unique physical properties, such as low density, high porosity, excellent mechanical stability, high hydrophobicity and superoleophilicity. PMID:24518262

  20. A fine-focusing x-ray source using carbon-nanofiber field emitter

    SciTech Connect

    Sugimoto, W.; Sugita, S.; Sakai, Y.; Goto, H.; Watanabe, Y.; Ohga, Y.; Kita, S.; Ohara, T.

    2010-08-15

    A fine-focusing x-ray source has been constructed employing a field electron emitter prepared by growing carbon-nanofibers (CNFs) on a metal tip. The x-ray source is composed of a CNF field electron emitter, an electrostatic lens, two magnetic lenses, and a W-target for generating x-rays by electron impact. The CNFs provided field electrons with a current density of J{approx}5x10{sup 9} A/m{sup 2}, which was evaluated with the aid of Fowler-Nordheim theory. The electron beam extracted from the CNF emitter was accelerated to the energies of E=10-25 keV, and then focused by the lenses. By recording the x-ray images of test charts, the optimum resolution of the x-ray source was estimated to be approximately D{sub x}=0.5 {mu}m.

  1. Mechanical Properties of Carbon Nanofiber Reinforced Polymer Composites-Molecular Dynamics Approach

    NASA Astrophysics Data System (ADS)

    Sharma, Sumit; Chandra, Rakesh; Kumar, Pramod; Kumar, Navin

    2016-06-01

    Molecular dynamics simulation has been used to study the effect of carbon nanofiber (CNF) volume fraction ( V f) and aspect ratio ( l/d) on mechanical properties of CNF-reinforced polypropylene (PP) composites. Materials Studio 5.5 has been used as a tool for finding the modulus and damping in composites. CNF composition in PP was varied by volume from 0% to 16%. The aspect ratio of CNF was varied from l/d = 5 to l/d = 100. Results show that, with only 2% addition by volume of CNF in PP, E 11 increases 748%. Increase in E 22 is much less in comparison to the increase in E 11. With the increase in the CNF aspect ratio ( l/d) up to l/d = 60, the longitudinal loss factor ( η 11) decreases rapidly. The results of this study have been compared with those available in the literature.

  2. Electrosorption of ions from aqueous solutions with carbon nanotubes and nanofibers composite film electrodes

    NASA Astrophysics Data System (ADS)

    Wang, X. Z.; Li, M. G.; Chen, Y. W.; Cheng, R. M.; Huang, S. M.; Pan, L. K.; Sun, Z.

    2006-07-01

    Electrosorption of ions from aqueous solutions with carbon nanotubes and nanofibers (CNTs-CNFs) composite film electrodes has been demonstrated. The large area CNTs-CNFs film was directly grown on Ni plate by low pressure and low temperature thermal chemical vapor deposition. The CNTs-CNFs electrodes have great advantages such as low cost, easy operation, long-term reproducibility, and integrity of monolithic CNTs-CNFs film and current collector. Batch-mode experiments at low voltage (0.4-2V) were conducted in a continuously recycling system to investigate the electrosorption process. Purification of water with good reproducibility was achieved because of optimal pore size distribution of CNTs-CNFs composite films.

  3. Structural characteristics of carbon nanofibers for on-chip interconnect applications

    SciTech Connect

    Ominami, Yusuke; Ngo, Quoc; Austin, Alexander J.; Yoong, Hans; Yang, Cary Y.; Cassell, Alan M.; Cruden, Brett A.; Li Jun; Meyyappan, M.

    2005-12-05

    In this letter, we compare the structures of plasma-enhanced chemical vapor deposition of Ni-catalyzed and Pd-catalyzed carbon nanofibers (CNFs) synthesized for on-chip interconnect applications with scanning transmission electron microscopy (STEM). The Ni-catalyzed CNF has a conventional fiberlike structure and many graphitic layers that are almost parallel to the substrate at the CNF base. In contrast, the Pd-catalyzed CNF has a multiwall nanotubelike structure on the sidewall spanning the entire CNF. The microstructure observed in the Pd-catalyzed fibers at the CNF-metal interface has the potential to lower contact resistance significantly, as our electrical measurements using current-sensing atomic force microscopy indicate. A structural model is presented based on STEM image analysis.

  4. Self-sensing of carbon nanofiber concrete columns subjected to reversed cyclic loading

    NASA Astrophysics Data System (ADS)

    Howser, R. N.; Dhonde, H. B.; Mo, Y. L.

    2011-08-01

    Civil infrastructures are generally a country's most expensive investment, and concrete is the most widely used material in the construction of civil infrastructures. During a structure's service life, concrete ages and deteriorates, leading to substantial loss of structural integrity and potentially resulting in catastrophic disasters such as highway bridge collapses. A solution for preventing such occurrences is the use of structural health monitoring (SHM) technology for concrete structures containing carbon nanofibers (CNF). CNF concrete has many structural benefits. CNF restricts the growth of nanocracks in addition to yielding higher strength and ductility. Additionally, test results indicate a relationship between electrical resistance and concrete strain, which can be well utilized for SHM. A series of reinforced concrete (RC) columns were built and tested under a reversed cyclic loading using CNF as a SHM device. The SHM device detected and assessed the level of damage in the RC columns, providing a real-time health monitoring system for the structure's overall integrity.

  5. Transfer of vertically aligned carbon nanofibers to polydimethylsiloxane (PDMS) while maintaining their alignment and impalefection functionality.

    PubMed

    Pearce, Ryan C; Railsback, Justin G; Anderson, Bryan D; Sarac, Mehmet F; McKnight, Timothy E; Tracy, Joseph B; Melechko, Anatoli V

    2013-02-01

    Vertically aligned carbon nanofibers (VACNFs) are synthesized on Al 3003 alloy substrates by direct current plasma-enhanced chemical vapor deposition. Chemically synthesized Ni nanoparticles were used as the catalyst for growth. The Si-containing coating (SiN(x)) typically created when VACNFs are grown on silicon was produced by adding Si microparticles prior to growth. The fiber arrays were transferred to PDMS by spin coating a layer on the grown substrates, curing the PDMS, and etching away the Al in KOH. The fiber arrays contain many fibers over 15 μm (long enough to protrude from the PDMS film and penetrate cell membranes) and SiN(x) coatings as observed by SEM, EDX, and fluorescence microscopy. The free-standing array in PDMS was loaded with pVENUS-C1 plasmid and human brain microcapillary endothelial (HBMEC) cells and was successfully impalefected. PMID:23281833

  6. Design and synthesis of superhydrophobic carbon nanofiber composite coatings for terahertz frequency shielding and attenuation

    NASA Astrophysics Data System (ADS)

    Das, Arindam; Megaridis, Constantine M.; Liu, Lei; Wang, Tao; Biswas, Abhijit

    2011-04-01

    We report design and synthesis of polymer-based large-area superhydrophobic carbon nanofiber (CNF) composite coatings for tunable electromagnetic interference shielding and attenuation in the terahertz (THz) frequency regime. Such coatings with different CNF/polymer weight ratios are characterized by a frequency domain THz spectroscopy system. A maximum THz shielding effectiveness of ˜32 dB was measured in the examined frequency range of 570-630 GHz. Coating attenuation level varied with CNF loading. Two-dimensional distributions of power attenuation at 600 GHz showed good spatial uniformity. The present composite coatings, in addition to their self-cleaning property, have high potential for advanced technology high-frequency applications.

  7. Optical limiting of high-repetition-rate laser pulses by carbon nanofibers suspended in polydimethylsiloxane

    NASA Astrophysics Data System (ADS)

    Videnichev, Dmitry A.; Belousova, Inna M.

    2014-06-01

    The optical limiting (OL) behavior of carbon nanofibers (CNFs) in polydimethylsiloxane (PDMS) was studied and compared with that of CNFs in water, and polyhedral multi-shell fullerene-like nanostructures (PMFNs) also in water. It was shown that when switching from single-shot to pulse-periodic regime of laser pulses (10 Hz), the CNF in PDMS suspension retains its OL characteristics, while in the aqueous suspensions, considerable degradation of OL characteristics is observed. It was also observed that a powerful laser pulse causes the CNF in PDMS suspension to become opaque for at least three seconds, while such a pulse brings out a bleaching effect in aqueous PMFN and CNF suspensions. The processes of OL degradation in aqueous suspensions, bleaching and darkening of the studied materials are discussed herein.

  8. Carbon nanofibers suppress fungal inhibition of seed germination of maize (Zea mays) and barley (Hordeum vulgare L.) crop

    NASA Astrophysics Data System (ADS)

    Joshi, Anjali; Sharma, Arti; Nayyar, Harsh; Verma, Gaurav; Dharamvir, Keya

    2015-08-01

    Carbon nanofibers (CNFs) are one of allotropes of carbon, consists of graphene layers arrangement in the form of stacked cones or like a cup diameter in nanometer and several millimeters in length. Their extraordinary mechanical, chemical and electronic properties are due to their small size. CNFs have been successfully applied in field of medicine in variety of diagnostic methods. They proven to be an excellent system for drug delivery, tissue regeneration, biosensor etc. This research focuses the applications of CNFs in all fields of Agriculture. In the we treated some fungal disease seed of maize and barley using functionalised CNFs. We find that the tested seeds grow just as well as the healthy seeds whereas the untreated fungal disease seeds, by themselves show very poor germination and seedling growth. This simple experiment shows the extraordinary ability of Carbon nanofibers in carrying effectively inside the germinated seeds.

  9. Carbon nanofibers suppress fungal inhibition of seed germination of maize (Zea mays) and barley (Hordeum vulgare L.) crop

    SciTech Connect

    Joshi, Anjali Sharma, Arti; Nayyar, Harsh; Verma, Gaurav; Dharamvir, Keya

    2015-08-28

    Carbon nanofibers (CNFs) are one of allotropes of carbon, consists of graphene layers arrangement in the form of stacked cones or like a cup diameter in nanometer and several millimeters in length. Their extraordinary mechanical, chemical and electronic properties are due to their small size. CNFs have been successfully applied in field of medicine in variety of diagnostic methods. They proven to be an excellent system for drug delivery, tissue regeneration, biosensor etc. This research focuses the applications of CNFs in all fields of Agriculture. In the we treated some fungal disease seed of maize and barley using functionalised CNFs. We find that the tested seeds grow just as well as the healthy seeds whereas the untreated fungal disease seeds, by themselves show very poor germination and seedling growth. This simple experiment shows the extraordinary ability of Carbon nanofibers in carrying effectively inside the germinated seeds.

  10. Reactive Melt Infiltration Of Silicon Into Porous Carbon

    NASA Technical Reports Server (NTRS)

    Behrendt, Donald R.; Singh, Mrityunjay

    1994-01-01

    Report describes study of synthesis of silicon carbide and related ceramics by reactive melt infiltration of silicon and silicon/molybdenum alloys into porous carbon preforms. Reactive melt infiltration has potential for making components in nearly net shape, performed in less time and at lower temperature. Object of study to determine effect of initial pore volume fraction, pore size, and infiltration material on quality of resultant product.

  11. TECHNICAL NOTE: A feasibility study of self-heating concrete utilizing carbon nanofiber heating elements

    NASA Astrophysics Data System (ADS)

    Chang, Christiana; Ho, Michelle; Song, Gangbing; Mo, Yi-Lung; Li, Hui

    2009-12-01

    This paper presents the development of an electric, self-heating concrete system that uses embedded carbon nanofiber paper as electric resistance heating elements. The proposed system utilizes the conductive properties of carbon fiber materials to heat a surface overlay of concrete with various admixtures to improve the concrete's thermal conductivity. The development and laboratory scale testing of the system were conducted for the various compositions of concrete containing, separately, carbon fiber, fly ash, and steel shavings as admixtures. The heating performances of these concrete mixtures with the carbon fiber heating element were experimentally obtained in a sub-freezing ambient environment in order to explore the use of such a system for deicing of concrete roadways. Analysis of electric power consumption, heating rate, and obtainable concrete surface temperatures under typical power loads was performed to evaluate the viability of a large scale implementation of the proposed heating system for roadway deicing applications. A cost analysis is presented to provide a comparison with traditional deicing methods, such as salting, and other integrated concrete heating systems.

  12. Strong magnetic field-assisted growth of carbon nanofibers and its microstructural transformation mechanism

    PubMed Central

    Luo, Chengzhi; Fu, Qiang; Pan, Chunxu

    2015-01-01

    It is well-known that electric and magnetic fields can control the growth direction, morphology and microstructure of one-dimensional carbon nanomaterials (1-DCNMs), which plays a key role for its potential applications in micro-nano-electrics and devices. In this paper, we introduce a novel process for controlling growth of carbon nanofibers (CNFs) with assistance of a strong magnetic field (up to 0.5 T in the center) in a chemical vapor deposition (CVD) system. The results reveal that: 1) The CNFs get bundled when grown in the presence of a strong magnetic field and slightly get aligned parallel to the direction of the magnetic field; 2) The CNFs diameter become narrowed and homogenized with increase of the magnetic field; 3) With the increase of the magnetic field, the microstructure of CNFs is gradually changed, i.e., the strong magnetic field makes the disordered “solid-cored” CNFs transform into a kind of bamboo-liked carbon nanotubes; 4) We propose a mechanism that the reason for these variations and transformation is due to diamagnetic property of carbon atoms, so that it has direction selectivity in the precipitation process. PMID:25761381

  13. Strong magnetic field-assisted growth of carbon nanofibers and its microstructural transformation mechanism.

    PubMed

    Luo, Chengzhi; Fu, Qiang; Pan, Chunxu

    2015-01-01

    It is well-known that electric and magnetic fields can control the growth direction, morphology and microstructure of one-dimensional carbon nanomaterials (1-DCNMs), which plays a key role for its potential applications in micro-nano-electrics and devices. In this paper, we introduce a novel process for controlling growth of carbon nanofibers (CNFs) with assistance of a strong magnetic field (up to 0.5 T in the center) in a chemical vapor deposition (CVD) system. The results reveal that: 1) The CNFs get bundled when grown in the presence of a strong magnetic field and slightly get aligned parallel to the direction of the magnetic field; 2) The CNFs diameter become narrowed and homogenized with increase of the magnetic field; 3) With the increase of the magnetic field, the microstructure of CNFs is gradually changed, i.e., the strong magnetic field makes the disordered "solid-cored" CNFs transform into a kind of bamboo-liked carbon nanotubes; 4) We propose a mechanism that the reason for these variations and transformation is due to diamagnetic property of carbon atoms, so that it has direction selectivity in the precipitation process. PMID:25761381

  14. Strong magnetic field-assisted growth of carbon nanofibers and its microstructural transformation mechanism

    NASA Astrophysics Data System (ADS)

    Luo, Chengzhi; Fu, Qiang; Pan, Chunxu

    2015-03-01

    It is well-known that electric and magnetic fields can control the growth direction, morphology and microstructure of one-dimensional carbon nanomaterials (1-DCNMs), which plays a key role for its potential applications in micro-nano-electrics and devices. In this paper, we introduce a novel process for controlling growth of carbon nanofibers (CNFs) with assistance of a strong magnetic field (up to 0.5 T in the center) in a chemical vapor deposition (CVD) system. The results reveal that: 1) The CNFs get bundled when grown in the presence of a strong magnetic field and slightly get aligned parallel to the direction of the magnetic field; 2) The CNFs diameter become narrowed and homogenized with increase of the magnetic field; 3) With the increase of the magnetic field, the microstructure of CNFs is gradually changed, i.e., the strong magnetic field makes the disordered ``solid-cored'' CNFs transform into a kind of bamboo-liked carbon nanotubes; 4) We propose a mechanism that the reason for these variations and transformation is due to diamagnetic property of carbon atoms, so that it has direction selectivity in the precipitation process.

  15. Development Trends in Porous Adsorbents for Carbon Capture.

    PubMed

    Sreenivasulu, Bolisetty; Sreedhar, Inkollu; Suresh, Pathi; Raghavan, Kondapuram Vijaya

    2015-11-01

    Accumulation of greenhouse gases especially CO2 in the atmosphere leading to global warming with undesirable climate changes has been a serious global concern. Major power generation in the world is from coal based power plants. Carbon capture through pre- and post- combustion technologies with various technical options like adsorption, absorption, membrane separations, and chemical looping combustion with and without oxygen uncoupling have received considerable attention of researchers, environmentalists and the stake holders. Carbon capture from flue gases can be achieved with micro and meso porous adsorbents. This review covers carbonaceous (organic and metal organic frameworks) and noncarbonaceous (inorganic) porous adsorbents for CO2 adsorption at different process conditions and pore sizes. Focus is also given to noncarbonaceous micro and meso porous adsorbents in chemical looping combustion involving insitu CO2 capture at high temperature (>400 °C). Adsorption mechanisms, material characteristics, and synthesis methods are discussed. Attention is given to isosteric heats and characterization techniques. The options to enhance the techno-economic viability of carbon capture techniques by integrating with CO2 utilization to produce industrially important chemicals like ammonia and urea are analyzed. From the reader's perspective, for different classes of materials, each section has been summarized in the form of tables or figures to get a quick glance of the developments. PMID:26422294

  16. A nucleation and growth model of vertically-oriented carbon nanofibers or nanotubes by plasma-enhanced catalytic chemical vapor deposition.

    PubMed

    Cojocaru, C S; Senger, A; Le Normand, F

    2006-05-01

    Carbon nanofibers are grown by direct current and hot filaments-activated catalytic chemical vapor deposition while varying the power of the hot filaments. Observations of these carbon nanofibers vertically oriented on a SiO2 (8 nm thick)/Si(100) substrate covered with Co nanoparticles (10-15 nm particle size) by Scanning Electron and Transmission Electron Microscopies show the presence of a graphitic "nest" either on the surface of the substrate or at the end of the specific nanofiber that does not encapsulate the catalytic particle. Strictly in our conditions, the activation by hot filaments is required to grow nanofibers with a C2H2 - H2 gas mixture, as large amounts of amorphous carbon cover the surface of the substrate without using hot filaments. From these observations as well as data of the literature, it is proposed that the nucleation of carbon nanofibers occurs through a complex process involving several steps: carbon concentration gradient starting from the catalytic carbon decomposition and diffusion from the surface of the catalytic nanoparticles exposed to the activated gas and promoted by energetic ionic species of the gas phase; subsequent graphitic condensation of a "nest" at the interface of the Co particle and substrate. The large concentration of highly reactive hydrogen radicals mainly provided by activation with hot filaments precludes further spreading out of this interfacial carbon nest over the entire surface of the substrate and thus selectively orientates the growth towards the condensation of graphene over facets that are perpendicular to the surface. Carbon nanofibers can then be grown within the well-known Vapor-Liquid-Solid process. Thus the effect of energetic ions and highly reactive neutrals like atomic hydrogen in the preferential etching of carbon on the edge of graphene shells and on the broadening of the carbon nanofiber is underlined. PMID:16792361

  17. Ionic Liquids as Versatile Precursors for Functionalized Porous Carbon and Carbon-Oxide Composite Materials by Confined Carbonization

    SciTech Connect

    Dai, Sheng; Wang, Xiqing

    2010-01-01

    Thermolysis of an ionic liquid (IL) gives no char residue, whereas heating the same IL trapped within an oxide framework affords high carbonization yields (see picture). This confinement method allows incorporation of heteroatoms from the parent IL in the final products, for the development of functionalized porous carbon and carbon-oxide composite materials.

  18. Hydrothermal synthesis of {beta}-nickel hydroxide nanocrystalline thin film and growth of oriented carbon nanofibers

    SciTech Connect

    Zhang Enlei; Tang Yuanhong; Zhang Yong; Guo Chi; Yang Lei

    2009-08-05

    Novel well-crystallized {beta}-nickel hydroxide nanocrystalline thin films were successfully synthesized at low temperature on the quartz substrates by hydrothermal method, and the oriented carbon nanofibers (CNFs) were prepared by acetylene cracking at 750 deg. C on thin film as the catalyst precursor. High resolution transmission electron microscopy (HR-TEM) measurement shows that thin films were constructed mainly with hexagonal {beta}-nickel hydroxide nanosheets. The average diameter of the nanosheets was about 80 nm and thickness about 15 nm. Hydrothermal temperature played an important role in the film growth process, influencing the morphologies and catalytic activity of the Ni catalysts. Ni thin films with high catalytic activity were obtained by reduction of these Ni(OH){sub 2} nanocrystalline thin films synthesized at 170 deg. C for 2 h in hydrothermal condition. The highest carbon yield was 1182%, and was significantly higher than the value of the catalyst precursor which was previously reported as the carbon yield (398%) for Ni catalysts. The morphology and growth mechanism of oriented CNFs were also studied finally.

  19. Copper/zinc bimetal nanoparticles-dispersed carbon nanofibers: A novel potential antibiotic material.

    PubMed

    Ashfaq, Mohammad; Verma, Nishith; Khan, Suphiya

    2016-02-01

    Copper (Cu) and zinc (Zn) nanoparticles (NPs) were asymmetrically distributed in carbon nanofibers (CNFs) grown on an activated carbon fiber (ACF) substrate by chemical vapor deposition (CVD). The CVD conditions were chosen such that the Cu NPs moved along with the CNFs during tip-growth, while the Zn NPs remained adhered at the ACF. The bimetal-ACF/CNF composite material was characterized by the metal NP release profiles, in-vitro hemolytic and antibacterial activities, and bacterial cellular disruption and adhesion assay. The synergetic effects of the bimetal NPs distributed in the ACFs/CNFs resulted from the relatively slower release of the Cu NPs located at the tip of the CNFs and faster release of the Zn NPs dispersed in the ACF. The Cu/Zn-grown ACFs/CNFs inhibited the growth of the Gram negative Escherichia coli, Gram positive Staphylococcus aureus, and Methicillin resistance Staphylococcus aureus bacterial strains, with superior efficiency (instant and prolonged inhibition) than the Cu or Zn single metal-grown ACFs/CNFs. The prepared bimetal-carbon composite material in this study has potential to be used in different biomedical applications such as wound healing and antibiotic wound dressing. PMID:26652451

  20. Growth of carbon nanofibers using resol-type phenolic resin and cobalt(II) catalyst.

    PubMed

    Kim, Taeyun; Mees, Karina; Park, Ho-Seon; Willert-Porada, Monika; Lee, Chang-Seop

    2013-11-01

    This study investigated carbon nanofibers (CNFs) grown on reticulated vitreous carbon (RVC) foam through catalytic deposition of ethylene. Before growing the CNFs, Co(II) on the RVC foam was expected to act as a catalyst by deposition. The preparation of the CNFs was a two-step process. The first step was preparing the RVC from polyurethane (PU) foam. Changes in weight over time were evaluated using two kinds of resol. The change in the mass and state of the sample with the change in temperature was studied during the carbonization process. The second step was to prepare the CNFs. An OH group was attached by the oxidation of the RVC foam. A change in the shape and mass of the sample was observed due to a change in nitric acid concentration and oxidation time. Then, cobalt was deposited to grow CNFs on the RVC foam. Hydrolysis helped to deposit the Co(ll) on the RVC foam. The appropriate time and temperature were investigated for the reduction process. In the last step, CNFs were prepared by the introducing ethylene gas. The resulting samples were analyzed using scanning electron microscopy, energy dispersive spectroscopy, N2-sorption, and X-ray photoelectron spectroscopy. PMID:24245253

  1. Consolidation of carbon nanofiber/copper composites by hot-pressing and spark plasma sintering: a comparative study.

    PubMed

    Barcena, Jorge; Martinez, Vladimir; Martinez, Ramon; Maudes, Jon; Sarries, Jose-Ignacio; Carol, Iñaki; Gonzalez, Javier-Jesus; Coleto, Javier

    2009-03-01

    Vapour grown carbon nanofibers have been incorporated into a copper matrix at 20 and 40 volume fractions. The manufacturing route involves the dispersion of the carbon nanofibers and their subsequent coating by electroless plating with copper. The consolidation of the composite powders was performed by two different techniques: hot-pressing and spark plasma sintering. A comparative study of the two processes is reported, in terms of microstructure, dispersion and porosity. The consolidation by hot-pressing (at 900 degrees C, 30 MPa) led to poreless composites (relative density > 96%) and to a homogeneous microstructure. On the other hand, spark plasma sintering (at 400 degrees C, 75 MPa) led to lower densification (relative density < 96%) and heterogeneous microstructure. PMID:19435042

  2. Effects of Carbonization Parameters of Moso-Bamboo-Based Porous Charcoal on Capturing Carbon Dioxide

    PubMed Central

    Jhan, Jhih-Wei; Cheng, Yi-Ming; Cheng, Hau-Hsein

    2014-01-01

    This study experimentally analyzed the carbon dioxide adsorption capacity of Moso-bamboo- (Phyllostachys edulis-) based porous charcoal. The porous charcoal was prepared at various carbonization temperatures and ground into powders with 60, 100, and 170 meshes, respectively. In order to understand the adsorption characteristics of porous charcoal, its fundamental properties, namely, charcoal yield, ash content, pH value, Brunauer-Emmett-Teller (BET) surface area, iodine number, pore volume, and powder size, were analyzed. The results show that when the carbonization temperature was increased, the charcoal yield decreased and the pH value increased. Moreover, the bamboo carbonized at a temperature of 1000°C for 2 h had the highest iodine sorption value and BET surface area. In the experiments, charcoal powders prepared at various carbonization temperatures were used to adsorb 1.854% CO2 for 120 h. The results show that the bamboo charcoal carbonized at 1000°C and ground with a 170 mesh had the best adsorption capacity, significantly decreasing the CO2 concentration to 0.836%. At room temperature and atmospheric pressure, the Moso-bamboo-based porous charcoal exhibited much better CO2 adsorption capacity compared to that of commercially available 350-mesh activated carbon. PMID:25225639

  3. Shape-Controlled Synthesis of Ni-Based Nanoparticles and Patterning for Carbon Nanofiber Growth

    NASA Astrophysics Data System (ADS)

    Sarac, Mehmet Fahri

    This dissertation reviews a comprehensive set of research results comprised of three studies, which includes the synthesis of nickel (Ni) nanoparticles (NPs) and their conversion chemistry, methods for depositing them onto substrates, and catalysis of carbon nanofiber growth. The first part of the work is concerned with the synthesis of Ni NPs, dropcasting and growing them in alignment with carbon nanofibers along a silicon (Si) substrate. Following observed success of this step, Ni NPs were airbrushed across different substrates, attempting to observe differences while reporting the results of an extensive comparative analysis of the different substrates used. Here, it was observed that the Ni NPs had a tendency to have dendritic rather than spherical shapes, motivating an additional study of the cause of branching and how it can be controlled. All three portions of this study are presented and discussed in detail. In the first set of experiments, vertically aligned carbon nanofibers (VACNFs) were created through ligand-stabilized Ni nanoparticle (NP) catalysts and plasma enhanced chemical vapor deposition; these NPs were used to allow growth of VACNFs in dense arrays. In the pregrowth heating process, the ligands are converted into graphitic shells that prevent agglomeration and coalescence of the catalyst NPs, resulting in a monodisperse VACNF size distribution. Meanwhile, VACNFs were grown from Ni NPs that had been airbrushed onto various substrates (silicon (Si), aluminum (Al), copper (Cu), and titanium (Ti)). Si micropowder was also used as a precursor for Si coatings formed in situ on VACNFs, causing rigidity. Growth of VACNFs on metal foils will facilitate applications that require thermal or electrical contact to the VACNFs, such as anode materials for Li-ion batteries and thermal interface materials. A related study focused on the synthesis of Ni3C1-x NPs, the control of branching in dendritic Ni3C1-x NPs and the effect of branching on the conversion into

  4. Heteroatom-doped highly porous carbon from human urine

    PubMed Central

    Chaudhari, Nitin Kaduba; Song, Min Young; Yu, Jong-Sung

    2014-01-01

    Human urine, otherwise potentially polluting waste, is an universal unused resource in organic form disposed by the human body. We present for the first time “proof of concept” of a convenient, perhaps economically beneficial, and innovative template-free route to synthesize highly porous carbon containing heteroatoms such as N, S, Si, and P from human urine waste as a single precursor for carbon and multiple heteroatoms. High porosity is created through removal of inherently-present salt particles in as-prepared “Urine Carbon” (URC), and multiple heteroatoms are naturally doped into the carbon, making it unnecessary to employ troublesome expensive pore-generating templates as well as extra costly heteroatom-containing organic precursors. Additionally, isolation of rock salts is an extra bonus of present work. The technique is simple, but successful, offering naturally doped conductive hierarchical porous URC, which leads to superior electrocatalytic ORR activity comparable to state of the art Pt/C catalyst along with much improved durability and methanol tolerance, demonstrating that the URC can be a promising alternative to costly Pt-based electrocatalyst for ORR. The ORR activity can be addressed in terms of heteroatom doping, surface properties and electrical conductivity of the carbon framework. PMID:24909133

  5. Pyrolytic carbon-coated silicon/carbon nanofiber composite anodes for high-performance lithium-ion batteries

    NASA Astrophysics Data System (ADS)

    Chen, Yanli; Hu, Yi; Shao, Jianzhong; Shen, Zhen; Chen, Renzhong; Zhang, Xiangwu; He, Xia; Song, Yuanze; Xing, Xiuli

    2015-12-01

    Pyrolytic carbon-coated Si/C nanofibers (Si/C-CNFs) composites have been prepared through the sucrose coating and secondary thermal treatment of Si/CNFs composites produced via electrospinning and carbonization. This results in a structure in which Si nanoparticles are distributed along the fibers, with the fiber surface being coated with an amorphous carbon layer through pyrolysis of the sucrose. This carbon coating not only limits the volume expansion of the exposed Si nanoparticles, preventing their direct contact with the electrolyte, but also creates a connection between the fibers that is beneficial to Li+ ion transport, structural integrity, and electrochemical conductivity. Consequently, the Si/C-CNFs composite exhibits a more stable cycle performance, better rate performance, and higher conductivity than Si/CNFs alone. The optimal level of performance was attained with a 20:200 mass ratio of sucrose to deionized water, with a high retained capacity of 1215.2 mAh g-1 after 50 cycles, thus indicating that it is a suitable anode material for Li-ion batteries.

  6. Mechanical, thermal and morphological characterization of polycarbonate/oxidized carbon nanofiber composites produced with a lean 2-step manufacturing process.

    PubMed

    Lively, Brooks; Kumar, Sandeep; Tian, Liu; Li, Bin; Zhong, Wei-Hong

    2011-05-01

    In this study we report the advantages of a 2-step method that incorporates an additional process pre-conditioning step for rapid and precise blending of the constituents prior to the commonly used melt compounding method for preparing polycarbonate/oxidized carbon nanofiber composites. This additional step (equivalent to a manufacturing cell) involves the formation of a highly concentrated solid nano-nectar of polycarbonate/carbon nanofiber composite using a solution mixing process followed by melt mixing with pure polycarbonate. This combined method yields excellent dispersion and improved mechanical and thermal properties as compared to the 1-step melt mixing method. The test results indicated that inclusion of carbon nanofibers into composites via the 2-step method resulted in dramatically reduced ( 48% lower) coefficient of thermal expansion compared to that of pure polycarbonate and 30% lower than that from the 1-step processing, at the same loading of 1.0 wt%. Improvements were also found in dynamic mechanical analysis and flexural mechanical properties. The 2-step approach is more precise and leads to better dispersion, higher quality, consistency, and improved performance in critical application areas. It is also consistent with Lean Manufacturing principles in which manufacturing cells are linked together using less of the key resources and creates a smoother production flow. Therefore, this 2-step process can be more attractive for industry. PMID:21780388

  7. Fabrication, structure, and magnetic properties of electrospun carbon/cobalt ferrite (C/CoFe2O4) composite nanofibers

    NASA Astrophysics Data System (ADS)

    Nilmoung, S.; Kidkhunthod, P.; Pinitsoontorn, S.; Rujirawat, S.; Yimnirun, R.; Maensiri, S.

    2015-04-01

    This work reports the fabrication and properties of carbon/cobalt ferrite (C/CoFe2O4) composite nanofibers by using electrospinning technique followed by carbonization process under mixed air and argon atmosphere. The as-prepared samples were characterized by means of thermogravimetric analysis, X-ray diffraction, scanning electron microscopy, transmission electron microscopy, Raman spectroscopy, X-ray absorption spectroscopy, and vibrating sample magnetometry. It was found that the structure of CoFe2O4 was cubic spinel with the variation of crystallite size between 22 and 54 nm depending on the magnetic source content. X-ray absorption near-edge spectra at the Fe (7,112 eV) and Co (7,709 eV) absorption K-edge were used to confirm the Fe3+ and Co2+ oxidation states of CoFe2O4 nanoparticles. The X-ray absorption fine structure analysis indicated that CoFe2O4 nanoparticles had a structure analogous to bulk-inverted spinel structure. All composite nanofibers exhibited ferromagnetic behavior related to the distribution of cations over tetrahedral and octahedral sites, whereas diamagnetic behavior was observed in pure carbon nanofibers. The magnetization was clearly enhanced with respect to the increase of magnetic source content, whereas the coercivity and the squareness ( M r/ M s) were dependent of crystallite size.

  8. Properties of equilibrium carbon dioxide hydrate in porous medium

    NASA Astrophysics Data System (ADS)

    Voronov, V. P.; Gorodetskii, E. E.; Podnek, V. E.; Grigoriev, B. A.

    2016-09-01

    Specific heat capacity, dissociation heat and hydration number of carbon dioxide hydrate in porous medium are determined by adiabatic calorimetry method. The measurements were carried out in the temperature range 250-290 K and in pressure range 1-5 MPa. The measured specific heat of the hydrate is approximately 2.7 J/(g K), which is significantly larger than the specific heat of methane hydrate. In particular, at heating, larger value of the specific heat of carbon dioxide hydrate is a result of gas emission from the hydrate. The hydration number at the hydrate-gas coexistence changes from 6.2 to 6.9. The dissociation heat of carbon dioxide hydrate varies from the 55 kJ/mol near the upper quadruple point to the 57 kJ/mol near the lower quadruple point.

  9. Boosting the local anodic oxidation of silicon through carbon nanofiber atomic force microscopy probes

    PubMed Central

    Lorenzoni, Matteo; Matsui, Soichiro; Tanemura, Masaki; Perez-Murano, Francesc

    2015-01-01

    Summary Many nanofabrication methods based on scanning probe microscopy have been developed during the last decades. Local anodic oxidation (LAO) is one of such methods: Upon application of an electric field between tip and surface under ambient conditions, oxide patterning with nanometer-scale resolution can be performed with good control of dimensions and placement. LAO through the non-contact mode of atomic force microscopy (AFM) has proven to yield a better resolution and tip preservation than the contact mode and it can be effectively performed in the dynamic mode of AFM. The tip plays a crucial role for the LAO-AFM, because it regulates the minimum feature size and the electric field. For instance, the feasibility of carbon nanotube (CNT)-functionalized tips showed great promise for LAO-AFM, yet, the fabrication of CNT tips presents difficulties. Here, we explore the use of a carbon nanofiber (CNF) as the tip apex of AFM probes for the application of LAO on silicon substrates in the AFM amplitude modulation dynamic mode of operation. We show the good performance of CNF-AFM probes in terms of resolution and reproducibility, as well as demonstration that the CNF apex provides enhanced conditions in terms of field-induced, chemical process efficiency. PMID:25671165

  10. NiCu Alloy Nanoparticle-Loaded Carbon Nanofibers for Phenolic Biosensor Applications

    PubMed Central

    Li, Dawei; Lv, Pengfei; Zhu, Jiadeng; Lu, Yao; Chen, Chen; Zhang, Xiangwu; Wei, Qufu

    2015-01-01

    NiCu alloy nanoparticle-loaded carbon nanofibers (NiCuCNFs) were fabricated by a combination of electrospinning and carbonization methods. A series of characterizations, including SEM, TEM and XRD, were employed to study the NiCuCNFs. The as-prepared NiCuCNFs were then mixed with laccase (Lac) and Nafion to form a novel biosensor. NiCuCNFs successfully achieved the direct electron transfer of Lac. Cyclic voltammetry and linear sweep voltammetry were used to study the electrochemical properties of the biosensor. The finally prepared biosensor showed favorable electrocatalytic effects toward hydroquinone. The detection limit was 90 nM (S/N = 3), the sensitivity was 1.5 µA µM−1, the detection linear range was 4 × 10−7–2.37 × 10−6 M. In addition, this biosensor exhibited satisfactory repeatability, reproducibility, anti-interference properties and stability. Besides, the sensor achieved the detection of hydroquinone in lake water. PMID:26610505

  11. Effect of filler surface properties on stress relaxation behavior of carbon nanofiber/polyurethane nanocomposites

    NASA Astrophysics Data System (ADS)

    Sedat Gunes, I.; Jimenez, Guillermo; Jana, Sadhan

    2009-03-01

    The effect of carbon nanofiber (CNF) surface properties on tensile stress relaxation behavior of CNF/polyurethane (PU) nanocomposites was analyzed. PU was synthesized from methylene diisocyanate, polypropylene glycol (PPG diol), and butanediol. CNF, oxidized CNF (ox-CNF), and PPG diol grafted CNF (ol-CNF) were selected as fillers. ol-CNF was obtained by grafting PPG diol onto ox-CNF by reacting it with the carboxyl groups present on ox-CNF surface. The atomic ratios of oxygen to carbon present on the filler surfaces were 0.13 and 0.18 on ox-CNF and on ol-CNF as compared to 0.015 on CNF, mostly due to the presence oxygen containing polar groups on the surfaces of the former. The composites were prepared by in-situ polymerization and melt mixing in a chaotic mixer. The stress relaxation behavior of composites was determined at room temperature after inducing a tensile strain of 100%. The presence of fillers augmented the rate of stress relaxation in composites which was highest in the presence of CNF. The results suggested that relatively weak polymer-filler interactions in composites of CNF promoted higher stress relaxation.

  12. Hierarchical Graphene-Containing Carbon Nanofibers for Lithium-Ion Battery Anodes.

    PubMed

    Dufficy, Martin K; Khan, Saad A; Fedkiw, Peter S

    2016-01-20

    We present a method to produce composite anodes consisting of thermally reduced graphene oxide-containing carbon nanofibers (TRGO/CNFs) via electrospinning a dispersion of polyacrylonitrile (PAN) and graphene oxide (GO) sheets in dimethylformamide followed by heat treatment at 650 °C. A range of GO (1-20 wt % GO relative to polymer concentration) was added to the polymer solution, with each sample comprising similar polymer chain packing and subsequent CNF microstructure, as assessed by X-ray diffraction. An increase from 0 to 20 wt % GO in the fibers led to carbonized nonwovens with enhanced electronic conductivity, as TRGO sheets conductively connected the CNFs. Galvanostatic half-cell cycling revealed that TRGO addition enhanced the specific discharge capacity of the fibers. The optimal GO concentration of 5 wt % GO enhanced first-cycle discharge capacities at C/24 rates (15.6 mA g(-1)) 150% compared to CNFs, with a 400% capacity increase at 2-C rates (750 mA g(-1)). We attribute the capacity enhancement to a high degree of GO exfoliation. The TRGO/CNFs also experienced no capacity fade after 200 cycles at 2-C rates. Impedance spectroscopy of the composite anodes demonstrated that charge-transfer resistances decreased as GO content increased, implying that high GO loadings result in more electrochemically active material. PMID:26704705

  13. Effects of the catalyst and substrate thickness on the carbon nanotubes/nanofibers as supercapacitor electrodes

    NASA Astrophysics Data System (ADS)

    Gao, Y.; Pandey, G. P.; Turner, J.; Westgate, C.; Sammakia, B.

    2012-12-01

    The different growth conditions of carbon nanotubes (CNTs)/carbon nanofibers (CNFs) which lead to different characteristics when used as supercapacitor electrodes are reported. A layer of SiO2 was coated onto the Si substrate and then a layer of Ti was evaporated as a current collector. CNTs/CNFs were synthesized on the Ti surface via a water-assisted chemical vapor deposition method at 800 °C and at atmospheric pressure utilizing iron (Fe) nanoparticles as catalysts, ethylene (C2H4) as the precursor gas and argon (Ar) and hydrogen (H2) as the carrier gases. The effects of different thicknesses of the catalyst (5 and 10 nm) and Ti substrate layer (10, 30 and 150 nm) on the specific capacitance of the CNFs were studied and the capacitance of the CNTs/CNFs-based device was dependent on CNT/CNF morphology of the CNFs that varied for different combinations of the catalyst and Ti layer thicknesses. The characterization of CNTs/CNFs was carried out using scanning electron microscopy, electron dispersive spectroscopy, transmission electron microscopy and electron diffraction. The specific capacitance was measured using cyclic voltammetry via a three-electrode system. The highest specific capacitance (60 F g-1) was obtained in the sample grown with 5 nm of Fe catalyst onto 10 nm of Ti substrate.

  14. Growth of High-Density Self-Aligned Carbon Nanotubes and Nanofibers Using Palladium Catalyst

    NASA Astrophysics Data System (ADS)

    Vollebregt, S.; Derakhshandeh, J.; Ishihara, R.; Wu, M. Y.; Beenakker, C. I. M.

    2010-04-01

    In this paper we demonstrate vertical self-aligned growth of carbon nanotubes (CNT) and carbon nanofibers (CNF) using 1 nm of Pd as the catalyst material. Results were compared with those obtained using traditional catalysts (Co, Fe, and Ni). Pd is of interest as it has been demonstrated to be an excellent material for electrical contact to nanotubes. CNT were grown using plasma-enhanced chemical vapor deposition (PECVD) at 450°C to 500°C and using atmospheric-pressure chemical vapor deposition (APCVD) between 450°C and 640°C. The results were investigated by scanning electron microscopy (SEM), transmission electron microscopy (TEM), and Raman spectroscopy. High-density (1011 cm-2 to 1012 cm-2) self-aligned CNT growth was obtained using APCVD and Pd as the catalyst, while Co and Fe resulted in random growth. TEM revealed that the CNT grown by Pd with PECVD form large bundles of tubes, while Ni forms large-diameter CNF. It was found that the CNT grown using Pd or Ni are of low quality compared with those grown by Co and Fe.

  15. Electrospun carbon nanofibers/electrocatalyst hybrids as asymmetric electrodes for vanadium redox flow battery

    NASA Astrophysics Data System (ADS)

    Wei, Guanjie; Fan, Xinzhuang; Liu, Jianguo; Yan, Chuanwei

    2015-05-01

    To improve the electrochemical activity of polyacrylonitrile (PAN)-based electrospun carbon nanofibers (ECNFs) toward vanadium redox couples, the multi-wall carbon nanotubes (CNTs) and Bi-based compound as electrocatalyst have been embedded in the ECNFs to make composite electrode, respectively. The morphology and electrochemical properties of pristine ECNFs, CNTs/ECNFs and Bi/ECNFs have been characterized. Among the three kinds of electrodes, the CNTs/ECNFs show best electrochemical activity toward VO2+/VO2+ redox couple, while the Bi/ECNFs present the best electrochemical activity toward V2+/V3+ redox couple. Furthermore, the high overpotential of hydrogen evolution on Bi/ECNFs makes the side-reaction suppressed. Because of the large property difference between the two composite electrodes, the CNTs/ECNFs and Bi/ECNFs are designed to act as positive and negative electrode for vanadium redox flow battery (VRFB), respectively. It not only does improve the kinetics of two electrode reactions at the same time, but also reduce the kinetics difference between them. Due to the application of asymmetric electrodes, performance of the cell is improved greatly.

  16. Direct synthesis of carbon nanofibers from South African coal fly ash

    PubMed Central

    2014-01-01

    Carbon nanofibers (CNFs), cylindrical nanostructures containing graphene, were synthesized directly from South African fly ash (a waste product formed during the combustion of coal). The CNFs (as well as other carbonaceous materials like carbon nanotubes (CNTs)) were produced by the catalytic chemical vapour deposition method (CCVD) in the presence of acetylene gas at temperatures ranging from 400°C to 700°C. The fly ash and its carbonaceous products were characterized by transmission electron microscopy (TEM), thermogravimetric analysis (TGA), laser Raman spectroscopy and Brunauer-Emmett-Teller (BET) surface area measurements. It was observed that as-received fly ash was capable of producing CNFs in high yield by CCVD, starting at a relatively low temperature of 400°C. Laser Raman spectra and TGA thermograms showed that the carbonaceous products which formed were mostly disordered. Small bundles of CNTs and CNFs observed by TEM and energy-dispersive spectroscopy (EDS) showed that the catalyst most likely responsible for CNF formation was iron in the form of cementite; X-ray diffraction (XRD) and Mössbauer spectroscopy confirmed these findings. PMID:25177215

  17. Porous nitrogen doped carbon fiber with churros morphology derived from electrospun bicomponent polymer as highly efficient electrocatalyst for Zn-air batteries

    NASA Astrophysics Data System (ADS)

    Park, Gi Su; Lee, Jang-Soo; Kim, Sun Tai; Park, Soojin; Cho, Jaephil

    2013-12-01

    Highly porous nitrogen doped carbon fibers like churros morphology are prepared from a simple and cost-effective fabrication process, electrospinning with bicomponent polymer consisting of polystyrene (PS) and polyacrylonitrile (PAN). From appropriate ratio of two polymer and pyrolysis at 1100 °C, newly churros morphology with extremely high surface area (1271 m2 g-1) is prepared. During carbonization, more unstable PS than PAN plays a critical role in forming such morphology by acting as sacrifice materials, thus providing additional formation of inner pores and outer etched surfaces. Furthermore, it demonstrates excellent electrocatalytic activity toward ORR, which is attributed to highly meso- and macro porous nitrogen-doped large surface area and enhanced graphitic-nitrogen groups of carbon fibers. For example, the performance of a Zn-air cell based on the nitrogen-doped porous carbon nanofibers exhibits a peak power density of 194 mW cm-2, comparable to that based on a commercial Pt/C catalyst (192 mW cm-2). Further, the generation of hydrogen peroxide ions (<20%) in a half cell is similar to that on the commercial Pt/C catalyst.

  18. Large surface area ordered porous carbons via nanocasting zeolite 10X and high performance for hydrogen storage application.

    PubMed

    Cai, Jinjun; Li, Liangjun; Lv, Xiaoxia; Yang, Chunpeng; Zhao, Xuebo

    2014-01-01

    We report the preparation of ordered porous carbons for the first time via nanocasting zeolite 10X with an aim to evaluate their potential application for hydrogen storage. The synthesized carbons exhibit large Brunauer-Emmett-Teller surface areas in the 1300-3331 m(2)/g range and pore volumes up to 1.94 cm(3)/g with a pore size centered at 1.2 nm. The effects of different synthesis processes with pyrolysis temperature varied in the 600-800 °C range on the surface areas, and pore structures of carbons were explored. During the carbonization process, carbons derived from the liquid-gas two-step routes at around 700 °C are nongraphitic and retain the particle morphology of 10X zeolite, whereas the higher pyrolysis temperature results in some graphitic domains and hollow-shell morphologies. In contrast, carbons derived from the direct acetylene infiltration process have some incident nanoribbon or nanofiber morphologies. A considerable hydrogen storage capacity of 6.1 wt % at 77 K and 20 bar was attained for the carbon with the surface area up to 3331 m(2)/g, one of the top-ranked capacities ever observed for large surface area adsorbents, demonstrating their potential uses for compacting gaseous fuels of hydrogen. The hydrogen capacity is comparable to those of previously reported values on other kinds of carbon-based materials and highly dependent on the surface area and micropore volume of carbons related to the optimum pore size, therefore providing guidance for the further search of nanoporous materials for hydrogen storage. PMID:24344972

  19. Free-Standing Thin Webs of Activated Carbon Nanofibers by Electrospinning for Rechargeable Li-O2 Batteries.

    PubMed

    Nie, Hongjiao; Xu, Chi; Zhou, Wei; Wu, Baoshan; Li, Xianfeng; Liu, Tao; Zhang, Huamin

    2016-01-27

    Free-standing activated carbon nanofibers (ACNF) were prepared through electrospinning combining with CO2 activation and then used for nonaqueous Li-O2 battery cathodes. As-prepared ACNF based cathode was loosely packed with carbon nanofibers complicatedly overlapped. Owing to some micrometer-sized pores between individual nanofibers, relatively high permeability of O2 across the cathode becomes feasible. Meanwhile, the mesopores introduced by CO2 activation act as additional nucleation sites for Li2O2 formation, leading to an increase in the density of Li2O2 particles along with a size decrease of the individual particles, and therefore, flake-like Li2O2 are preferentially formed. In addition, the free-standing structure of ACNF cathode eliminates the side reactions about PVDF. As a result, the Li-O2 batteries with ACNF cathodes showed increased discharge capacities, reduced overpotentials, and longer cycle life in the case of full discharge and charge operation. This provides a novel pathway for the design of cathodes for Li-O2 battery. PMID:26691321

  20. An inner filter effect based sensor of tetracycline hydrochloride as developed by loading photoluminescent carbon nanodots in the electrospun nanofibers.

    PubMed

    Lin, Min; Zou, Hong Yan; Yang, Tong; Liu, Ze Xi; Liu, Hui; Huang, Cheng Zhi

    2016-02-01

    The inner filter effect (IFE), which results from the absorption of the excitation or emission light by absorbers, has been employed as an alternative approach in sensing systems due to its flexibility and simplicity. In this work, highly photoluminescent carbon nanodots (CDs), which were simply prepared through a new one-step microwave synthesis route, were loaded in electrospun nanofibers, and the obtained nanofibers were then successfully applied to develop a fluorescent IFE-based visual sensor for tetracycline hydrochloride (Tc) sensing in milk. This developed visual sensor has high selectivity owing to the requirements of the spectral overlap between the CDs and Tc, showing high promise in sensing chemistry with an efficient response and economic effect. PMID:26781447

  1. Fabrication and characterization of polylactic acid and polylactic acid/multi-walled carbon nanotube nanofibers through centrifugal spinning

    NASA Astrophysics Data System (ADS)

    Patlan, Richard

    Biocompatible polymer nanofibers hold great potential in the biomedical engineering field. Their biodegradable nature and enhanced properties could help solve a wide array of health related problems, particularly in the areas of tissue regeneration, drug delivery, and biosensor design. The novel Forcespinning™ method allows the production of submicron fibers without many of the drawbacks found in electrospinning, while also providing a substantial increase in fiber production. The aim of the study was to utilize this method to fabricate non-woven nanofibrous mats composed of polylactic acid (PLA) and polylactic acid/multi-walled carbon nanotube composite fibers. The morphology, thermal properties, and crystalline structure of the resulting nanofibers were then characterized using Scanning Electron Microscopy (SEM), Transmission Electron Microscopy (TEM), Thermogravimetric Analysis (TGA), Differential Scanning Calorimetry (DSC), and X-Ray Diffraction (XRD).

  2. Graphene nanoribbons hybridized carbon nanofibers: remarkably enhanced graphitization and conductivity, and excellent performance as support material for fuel cell catalysts

    NASA Astrophysics Data System (ADS)

    Wang, Chaonan; Gao, Hongrong; Li, Hong; Zhang, Yiren; Huang, Bowen; Zhao, Junhong; Zhu, Yan; Yuan, Wang Zhang; Zhang, Yongming

    2014-01-01

    High electronic conductivity of the support material and uniform distribution of the catalyst nanoparticles (NPs) are extremely desirable for electrocatalysts. In this paper, we present our recent progress on electrocatalysts for fuel cells with simultaneously improved conductivity of the supporting carbon nanofibers (CNFs) and distribution of platinum (Pt) NPs through facile incorporation of graphene nanoribbons (GNRs). Briefly, GNRs were obtained by the cutting and unzipping of multiwalled carbon nanotubes (MWCNTs) and subsequent thermal reduction and were first used as novel nanofillers in CNFs towards high performance support material for electrocatalysis. Through electrospinning and carbonization processes, GNR embedded carbon nanofibers (G-CNFs) with greatly enhanced graphitization and electronic conductivity were synthesized. Chemical deposition of Pt NPs onto G-CNFs generated a new Pt-G-CNF hybrid catalyst, with homogeneously distributed Pt NPs of ~3 nm. Compared to Pt-CNF (Pt on pristine CNFs) and Pt-M-CNF (Pt on MWCNT embedded CNFs), Pt-G-CNF hybrids exhibit significantly improved electrochemically active surface area (ECSA), better CO tolerance for electro-oxidation of methanol and higher electrochemical stability, testifying G-CNFs are promising support materials for high performance electrocatalysts for fuel cells.High electronic conductivity of the support material and uniform distribution of the catalyst nanoparticles (NPs) are extremely desirable for electrocatalysts. In this paper, we present our recent progress on electrocatalysts for fuel cells with simultaneously improved conductivity of the supporting carbon nanofibers (CNFs) and distribution of platinum (Pt) NPs through facile incorporation of graphene nanoribbons (GNRs). Briefly, GNRs were obtained by the cutting and unzipping of multiwalled carbon nanotubes (MWCNTs) and subsequent thermal reduction and were first used as novel nanofillers in CNFs towards high performance support material for

  3. An inner filter effect based sensor of tetracycline hydrochloride as developed by loading photoluminescent carbon nanodots in the electrospun nanofibers

    NASA Astrophysics Data System (ADS)

    Lin, Min; Zou, Hong Yan; Yang, Tong; Liu, Ze Xi; Liu, Hui; Huang, Cheng Zhi

    2016-01-01

    The inner filter effect (IFE), which results from the absorption of the excitation or emission light by absorbers, has been employed as an alternative approach in sensing systems due to its flexibility and simplicity. In this work, highly photoluminescent carbon nanodots (CDs), which were simply prepared through a new one-step microwave synthesis route, were loaded in electrospun nanofibers, and the obtained nanofibers were then successfully applied to develop a fluorescent IFE-based visual sensor for tetracycline hydrochloride (Tc) sensing in milk. This developed visual sensor has high selectivity owing to the requirements of the spectral overlap between the CDs and Tc, showing high promise in sensing chemistry with an efficient response and economic effect.The inner filter effect (IFE), which results from the absorption of the excitation or emission light by absorbers, has been employed as an alternative approach in sensing systems due to its flexibility and simplicity. In this work, highly photoluminescent carbon nanodots (CDs), which were simply prepared through a new one-step microwave synthesis route, were loaded in electrospun nanofibers, and the obtained nanofibers were then successfully applied to develop a fluorescent IFE-based visual sensor for tetracycline hydrochloride (Tc) sensing in milk. This developed visual sensor has high selectivity owing to the requirements of the spectral overlap between the CDs and Tc, showing high promise in sensing chemistry with an efficient response and economic effect. Electronic supplementary information (ESI) available: Experimental section and additional figures (Fig. S1-S9). See DOI: 10.1039/c5nr08177g

  4. Occupational Exposure Assessment in Carbon Nanotube and Nanofiber Primary and Secondary Manufacturers

    PubMed Central

    DAHM, MATTHEW M.; EVANS, DOUGLAS E.; SCHUBAUER-BERIGAN, MARY K.; BIRCH, M. EILEEN; FERNBACK, JOSEPH E.

    2015-01-01

    Research Significance Toxicological evidence suggests the potential for a wide range of health effects, which could result from exposure to carbon nanotubes (CNTs) and carbon nanofibers (CNFs). The National Institute for Occupational Safety and Health (NIOSH) has proposed a recommended exposure limit (REL) for CNTs/CNFs at the respirable size fraction. The current literature is lacking exposure information, with few studies reporting results for personal breathing zone (PBZ) samples in occupational settings. To address this gap, exposure assessments were conducted at six representative sites identified as CNT/CNF primary or secondary manufacturers. Methods Personal and area filter-based samples were collected for both the inhalable mass concentration and the respirable mass concentration of elemental carbon (EC) as well as CNT structure count analysis by transmission electron microscopy to assess exposures. When possible, full-shift PBZ samples were collected; area samples were collected on a task-based approach. Results The vast majority of samples collected in this study were below the proposed REL (7 μg m−3). Two of the three secondary manufacturers’ surveyed found concentrations above the proposed REL. None of the samples collected at primary manufacturers were found to be above the REL. Visual and microscopy-based evidence of CNTs/CNFs were found at all sites, with the highest CNT/CNF structure counts being found in samples collected at secondary manufacturing sites. The statistical correlations between the filter-based samples for the mass concentration of EC and CNT structure counts were examined. A general trend was found with a P-value of 0.01 and a corresponding Pearson correlation coefficient of 0.44. Conclusions CNT/CNF concentrations were above the proposed NIOSH REL for PBZ samples in two secondary manufacturing facilities that use these materials for commercial applications. These samples were collected during dry powder handling processes, such

  5. Synthesis and Application of Si/Carbon Nanofiber Composites Based on Ni and Mo Catalysts for Anode Material of Lithium Secondary Batteries.

    PubMed

    Jang, Eunyi; Park, Heal-Ku; Lee, Chang-Seop

    2016-05-01

    In this paper, carbon nanofibers (CNFs) and Si/carbon nanofiber composites were synthesized for use as the anode material of lithium secondary batteries. Catalysts were prepared based on Ni and Mo metals and CNFs were grown through chemical vapor deposition (CVD). In addition, the grown CNFs were mixed with silicon particles to synthesize Si/carbon nanofibers composites. The physiochemical characteristics of the synthesized CNFs and Si/carbon nanofiber composites were analyzed by SEM, EDS, XRD, Raman, BET and XPS. The electrochemical characteristics were investigated by using cyclic voltammetry and galvanostatic charge-discharge. Using CNFs and Si/carbon nanofiber composites as the anode material, three electrode cells were assembled and the electrochemical characteristics were measured using LiPF6 and LiClO4 as electrolytes. As a result of the galvanostatic charge-discharge of CNFs that were grown through catalysts with Ni and Mo concentration ratio of 6:4, the initial discharge capacity when using LiPF6 as the electrolyte was 570 mAh/g and the retention rate was 15.05%. In the case of using LiClO4 as the electrolyte, the initial discharge capacity was 263 mAh/g and the retention rate was 67.23%. PMID:27483824

  6. Preparation of novel carbon microfiber/carbon nanofiber-dispersed polyvinyl alcohol-based nanocomposite material for lithium-ion electrolyte battery separator.

    PubMed

    Sharma, Ajit K; Khare, Prateek; Singh, Jayant K; Verma, Nishith

    2013-04-01

    A novel nanocomposite polyvinyl alcohol precursor-based material dispersed with the web of carbon microfibers and carbon nanofibers is developed as lithium (Li)-ion electrolyte battery separator. The primary synthesis steps of the separator material consist of esterification of polyvinyl acetate to produce polyvinyl alcohol gel, ball-milling of the surfactant dispersed carbon micro-nanofibers, mixing of the milled micron size (~500 nm) fibers to the reactant mixture at the incipience of the polyvinyl alcohol gel formation, and the mixing of hydrophobic reagents along with polyethylene glycol as a plasticizer, to produce a thin film of ~25 μm. The produced film, uniformly dispersed with carbon micro-nanofibers, has dramatically improved performance as a battery separator, with the ion conductivity of the electrolytes (LiPF6) saturated film measured as 0.119 S-cm(-1), approximately two orders of magnitude higher than that of polyvinyl alcohol. The other primary characteristics of the produced film, such as tensile strength, contact angle, and thermal stability, are also found to be superior to the materials made of other precursors, including polypropylene and polyethylene, discussed in the literature. The method of producing the films in this study is novel, simple, environmentally benign, and economically viable. PMID:23827627

  7. Novel injectable biomimetic hydrogels with carbon nanofibers and self assembled rosette nanotubes for myocardial applications.

    PubMed

    Meng, Xiangling; Stout, David A; Sun, Linlin; Beingessner, Rachel L; Fenniri, Hicham; Webster, Thomas J

    2013-04-01

    The objective of the present in vitro study was to investigate cardiomyocyte functions, specifically their adhesion and proliferation, on injectable scaffolds containing RNT (rosette nanotubes) and CNF (carbon nanofibers) in a pHEMA (poly(2-hydroxyethyl methacrylate)) hydrogel to determine their potential for myocardial tissue engineering applications. RNTs are novel biocompatible nanomaterials assembled from synthetic analogs of DNA bases guanine and cytosine that self-assemble within minutes when placed in aqueous solutions at body temperatures. These materials could potentially improve cardiomyocyte functions and solidification time of pHEMA and CNF composites. Because heart tissue is conductive, CNFs were added to pHEMA to increase the composite's conductivity. Our results showed that cardiomyocyte density increased after 4 h, 1 day, and 3 days with greater amounts of CNFs and greater amounts of RNTs in pHEMA (up to 10 mg mL(-1) CNFs and 0.05 mg mL(-1) RNTs). Factors that may have increased cardiomyocyte functions include greater wettability, conductivity, and an increase in surface nanoroughness with greater amounts of CNFs and RNTs. In effect, contact angles measured on the surface of the composites decreased while the conductivity and surface roughness increased as CNFs and RNTs content increased. Lastly, the ultimate tensile modulus decreased for composites with greater amounts of CNFs. In summary, the properties of these injectable composites make them promising candidates for myocardial tissue engineering applications and should be further studied. PMID:23008178

  8. Hierarchically mesoporous CuO/carbon nanofiber coaxial shell-core nanowires for lithium ion batteries

    PubMed Central

    Park, Seok-Hwan; Lee, Wan-Jin

    2015-01-01

    Hierarchically mesoporous CuO/carbon nanofiber coaxial shell-core nanowires (CuO/CNF) as anodes for lithium ion batteries were prepared by coating the Cu2(NO3)(OH)3 on the surface of conductive and elastic CNF via electrophoretic deposition (EPD), followed by thermal treatment in air. The CuO shell stacked with nanoparticles grows radially toward the CNF core, which forms hierarchically mesoporous three-dimensional (3D) coaxial shell-core structure with abundant inner spaces in nanoparticle-stacked CuO shell. The CuO shells with abundant inner spaces on the surface of CNF and high conductivity of 1D CNF increase mainly electrochemical rate capability. The CNF core with elasticity plays an important role in strongly suppressing radial volume expansion by inelastic CuO shell by offering the buffering effect. The CuO/CNF nanowires deliver an initial capacity of 1150 mAh g−1 at 100 mA g−1 and maintain a high reversible capacity of 772 mAh g−1 without showing obvious decay after 50 cycles. PMID:25944615

  9. Carbon nanofibers arrays: A novel tool for microdelivery of biomolecules to plants

    DOE PAGESBeta

    Davern, Sandra M.; McKnight, Timothy E.; Kalluri, Udaya C.; Standaert, Robert F.; Mirzadeh, Saed; Greenberg, Jean T.; Jelenska, Joanna; Shpak, Elena D.; Morrell-Falvey, Jennifer L.

    2016-04-27

    Effective methods for delivering bioprobes into the cells of intact plants are essential for investigating diverse biological processes. Increasing research on trees, such as Populus spp., for bioenergy applications is driving the need for techniques that work well with tree species. This report introduces vertically aligned carbon nanofiber (VACNF) arrays as a new tool for microdelivery of labeled molecules to Populus leaf tissue and whole plants. We demonstrated that VACNFs penetrate the leaf surface to deliver sub-microliter quantities of solution containing fluorescent or radiolabeled molecules into Populus leaf cells. Importantly, VACNFs proved to be gentler than abrasion with carborundum, amore » common way to introduce material into leaves. Unlike carborundum, VACNFs did not disrupt cell or tissue integrity, nor did they induce production of hydrogen peroxide, a typical wound response. We show that femtomole to picomole quantities of labeled molecules (fluorescent dyes, small proteins and dextran), ranging from 0.5–500 kDa, can be introduced by VACNFs, and we demonstrate the use of the approach to track delivered probes from their site of introduction on the leaf to distal plant regions. VACNF arrays thus offer an attractive microdelivery method for the introduction of biomolecules and other probes into trees and potentially other types of plants.« less

  10. Heterometal nanoparticles from Ru-based molecular clusters covalently anchored onto functionalized carbon nanotubes and nanofibers

    PubMed Central

    Vidick, Deborah; Ke, Xiaoxing; Devillers, Michel; Poleunis, Claude; Delcorte, Arnaud; Moggi, Pietro; Van Tendeloo, Gustaaf

    2015-01-01

    Summary Heterometal clusters containing Ru and Au, Co and/or Pt are anchored onto carbon nanotubes and nanofibers functionalized with chelating phosphine groups. The cluster anchoring yield is related to the amount of phosphine groups available on the nanocarbon surface. The ligands of the anchored molecular species are then removed by gentle thermal treatment in order to form nanoparticles. In the case of Au-containing clusters, removal of gold atoms from the clusters and agglomeration leads to a bimodal distribution of nanoparticles at the nanocarbon surface. In the case of Ru–Pt species, anchoring occurs without reorganization through a ligand exchange mechanism. After thermal treatment, ultrasmall (1–3 nm) bimetal Ru–Pt nanoparticles are formed on the surface of the nanocarbons. Characterization by high resolution transmission electron microscopy (HRTEM) and high angle annular dark field scanning transmission electron microscopy (HAADF-STEM) confirms their bimetal nature on the nanoscale. The obtained bimetal nanoparticles supported on nanocarbon were tested as catalysts in ammonia synthesis and are shown to be active at low temperature and atmospheric pressure with very low Ru loading. PMID:26199832

  11. Electrophoretic nanotechnology of graphene-carbon nanotube and graphene-polypyrrole nanofiber composites for electrochemical supercapacitors.

    PubMed

    Shi, Kaiyuan; Zhitomirsky, Igor

    2013-10-01

    Thin films of multiwalled carbon nanotubes (MWCNT), graphene and polypyrrole (PPy) nanofibers were prepared by cathodic electrophoretic deposition (EPD) from aqueous suspensions, containing safranin (SAF) as a new dispersant. The results of Fourier transform infrared spectroscopy, UV-Vis spectroscopy studies and sedimentation tests, coupled with deposition yield and electron microscopy data showed that SAF adsorbed on MWCNT, graphene and PPy, provided their dispersion and charging in the suspensions and allowed efficient EPD. The deposition yield can be controlled by the variation of SAF concentration in the suspensions and deposition time. The use of SAF as a co-dispersant for MWCNT, graphene and PPy, allowed controlled EPD of composite graphene-MWCNT and graphene-PPy films. The proposed approach for the deposition of PPy paves the way for EPD of neutral polymers using organic dyes as dispersing and charging agents. The composite films were investigated for application in electrochemical supercapacitors (ES). The graphene-MWCNT and graphene-PPy films showed significant increase in capacitance, decrease in resistance and increase in capacitance retention at high charge-discharge rates compared to the films of individual components. The analysis of electrochemical testing results and electron microscopy data provided an insight into the influence of composite microstructure on electrochemical performance. The composites, prepared by EPD are promising materials for electrodes of ES. PMID:23880521

  12. Higher-power supercapacitor electrodes based on mesoporous manganese oxide coating on vertically aligned carbon nanofibers.

    PubMed

    Klankowski, Steven A; Pandey, Gaind P; Malek, Gary; Thomas, Conor R; Bernasek, Steven L; Wu, Judy; Li, Jun

    2015-05-14

    A study on the development of high-power supercapacitor materials based on formation of thick mesoporous MnO2 shells on a highly conductive 3D template using vertically aligned carbon nanofibers (VACNFs). Coaxial manganese shells of 100 to 600 nm nominal thicknesses are sputter-coated on VACNFs and then electrochemically oxidized into rose-petal-like mesoporous MnO2 structure. Such a 3D MnO2/VACNF hybrid architecture provides enhanced ion diffusion throughout the whole MnO2 shell and yields excellent current collection capability through the VACNF electrode. These two effects collectively enable faster electrochemical reactions during charge-discharge of MnO2 in 1 M Na2SO4. Thick MnO2 shells (up to 200 nm in radial thickness) can be employed, giving a specific capacitance up to 437 F g(-1). More importantly, supercapacitors employing such a 3D MnO2/VACNF hybrid electrode illustrate more than one order of magnitude higher specific power than the state-of-the-art ones based on other MnO2 structures, reaching ∼240 kW kg(-1), while maintaining a comparable specific energy in the range of 1 to 10 Wh kg(-1). This hybrid approach demonstrates the potential of 3D core-shell architectures for high-power energy storage devices. PMID:25894255

  13. Lithium aluminosilicate reinforced with carbon nanofiber and alumina for controlled-thermal-expansion materials

    NASA Astrophysics Data System (ADS)

    Borrell, Amparo; García-Moreno, Olga; Torrecillas, Ramón; García-Rocha, Victoria; Fernández, Adolfo

    2012-02-01

    Materials with a very low or tailored thermal expansion have many applications ranging from cookware to the aerospace industry. Among others, lithium aluminosilicates (LAS) are the most studied family with low and negative thermal expansion coefficients. However, LAS materials are electrical insulators and have poor mechanical properties. Nanocomposites using LAS as a matrix are promising in many applications where special properties are achieved by the addition of one or two more phases. The main scope of this work is to study the sinterability of carbon nanofiber (CNFs)/LAS and CNFs/alumina/LAS nanocomposites, and to adjust the ratio among components for obtaining a near-zero or tailored thermal expansion. Spark plasma sintering of nanocomposites, consisting of commercial CNFs and alumina powders and an ad hoc synthesized β-eucryptite phase, is proposed as a solution to improving mechanical and electrical properties compared with the LAS ceramics obtained under the same conditions. X-ray diffraction results on phase compositions and microstructure are discussed together with dilatometry data obtained in a wide temperature range (-150 to 450 °C). The use of a ceramic LAS phase makes it possible to design a nanocomposite with a very low or tailored thermal expansion coefficient and exceptional electrical and mechanical properties.

  14. Electrochemically Active Polyaniline (PANi) Coated Carbon Nanopipes and PANi Nanofibers Containing Composite.

    PubMed

    Ramana, G Venkata; Kumar, P Sampath; Srikanth, Vadali V S S; Padya, Balaji; Jain, P K

    2015-02-01

    A composite constituted by carbon nanopipes (CNPs) and polyaniline nanofibers (PANi NFs) is synthesized using in-situ chemical oxidative polymerization. Owing to its electrochemical activity the composite is found to be suitable as a working electrode material in hybrid type supercapacitors. Microstructural and phase analyses of the composite showed that (i) CNP surfaces are coated with PANi and (ii) PANi coated CNPs are distributed among PANi NFs. The composite shows an excellent electrochemical activity and a high specific capacitance of ~224.39 F/g. The electro-chemical activity of the composite is explicated in correlation with crystallinity, intrinsic oxidation state, and doping degree of PANi in the composite. The electro-chemical activity of the composite is also explicated in correlation with BET surface area and ordered meso-porosity pertaining to the composite. Charge/discharge curves indicate that the specific capacitance of the composite is a result of electric double-layer capacitance offered by CNPs and Faradaic pseudo capacitance offered by PANi NFs. PMID:26353652

  15. Structure and electrochemical applications of boron-doped graphitized carbon nanofibers

    NASA Astrophysics Data System (ADS)

    Yeo, Jae-Seong; Jang, Sang-Min; Miyawaki, Jin; An, Bai; Mochida, Isao; Rhee, Choong Kyun; Yoon, Seong-Ho

    2012-08-01

    Boron-doped graphitized carbon nanofibers (CNFs) were prepared by optimizing CNFs preparation, surface treatment, graphitization and boron-added graphitization. The interlayer spacing (d002) of the boron-doped graphitized CNFs reached 3.356 Å, similar to that of single-crystal graphite. Special platelet CNFs (PCNFs), for which d002 is less than 3.400 Å, were selected for further heat treatment. The first heat treatment of PCNFs at 2800 °C yielded a d002 between 3.357 and 3.365 Å. Successive nitric acid treatment and a second heat treatment with boric acid reduced d002 to 3.356 Å. The resulting boron-doped PCNFs exhibited a high discharge capacity of 338 mAh g-1 between 0 and 0.5 V versus Li/Li+ and 368 mAh g-1 between 0 and 1.5 V versus Li/Li+. The first-cycle Coulombic efficiency was also enhanced to 71-80%. Such capacity is comparable to that of natural graphite under the same charge/discharge conditions. The boron-doped PCNFs also exhibited improved rate performance with twice the capacity of boron-doped natural graphite at a discharge rate of 5 C.

  16. Structure and electrochemical applications of boron-doped graphitized carbon nanofibers.

    PubMed

    Yeo, Jae-Seong; Jang, Sang-Min; Miyawaki, Jin; An, Bai; Mochida, Isao; Rhee, Choong Kyun; Yoon, Seong-Ho

    2012-08-10

    Boron-doped graphitized carbon nanofibers (CNFs) were prepared by optimizing CNFs preparation, surface treatment, graphitization and boron-added graphitization. The interlayer spacing (d₀₀₂) of the boron-doped graphitized CNFs reached 3.356 Å, similar to that of single-crystal graphite. Special platelet CNFs (PCNFs), for which d₀₀₂ is less than 3.400 Å, were selected for further heat treatment. The first heat treatment of PCNFs at 2800 °C yielded a d₀₀₂ between 3.357 and 3.365 Å. Successive nitric acid treatment and a second heat treatment with boric acid reduced d₀₀₂ to 3.356 Å. The resulting boron-doped PCNFs exhibited a high discharge capacity of 338 mAh g⁻¹ between 0 and 0.5 V versus Li/Li⁺ and 368 mAh g⁻¹ between 0 and 1.5 V versus Li/Li⁺. The first-cycle Coulombic efficiency was also enhanced to 71-80%. Such capacity is comparable to that of natural graphite under the same charge/discharge conditions. The boron-doped PCNFs also exhibited improved rate performance with twice the capacity of boron-doped natural graphite at a discharge rate of 5 C. PMID:22797214

  17. Carbon Nanofiber Nanoelectrodes for Neural Stimulation and Chemical Detection: The Era of Smart Deep Brain Stimulation

    NASA Technical Reports Server (NTRS)

    Koehne, Jessica E.

    2016-01-01

    A sensor platform based on vertically aligned carbon nanofibers (CNFs) has been developed. Their inherent nanometer scale, high conductivity, wide potential window, good biocompatibility and well-defined surface chemistry make them ideal candidates as biosensor electrodes. Here, we report two studies using vertically aligned CNF nanoelectrodes for biomedical applications. CNF arrays are investigated as neural stimulation and neurotransmitter recording electrodes for application in deep brain stimulation (DBS). Polypyrrole coated CNF nanoelectrodes have shown great promise as stimulating electrodes due to their large surface area, low impedance, biocompatibility and capacity for highly localized stimulation. CNFs embedded in SiO2 have been used as sensing electrodes for neurotransmitter detection. Our approach combines a multiplexed CNF electrode chip, developed at NASA Ames Research Center, with the Wireless Instantaneous Neurotransmitter Concentration Sensor (WINCS) system, developed at the Mayo Clinic. Preliminary results indicate that the CNF nanoelectrode arrays are easily integrated with WINCS for neurotransmitter detection in a multiplexed array format. In the future, combining CNF based stimulating and recording electrodes with WINCS may lay the foundation for an implantable "smart" therapeutic system that utilizes neurochemical feedback control while likely resulting in increased DBS application in various neuropsychiatric disorders. In total, our goal is to take advantage of the nanostructure of CNF arrays for biosensing studies requiring ultrahigh sensitivity, high-degree of miniaturization, and selective biofunctionalization.

  18. Carbon Nanofiber Arrays: A Novel Tool for Microdelivery of Biomolecules to Plants

    PubMed Central

    Davern, Sandra M.; McKnight, Timothy E.; Morrell-Falvey, Jennifer L.; Shpak, Elena D.; Kalluri, Udaya C.; Jelenska, Joanna; Greenberg, Jean T.; Mirzadeh, Saed

    2016-01-01

    Effective methods for delivering bioprobes into the cells of intact plants are essential for investigating diverse biological processes. Increasing research on trees, such as Populus spp., for bioenergy applications is driving the need for techniques that work well with tree species. This report introduces vertically aligned carbon nanofiber (VACNF) arrays as a new tool for microdelivery of labeled molecules to Populus leaf tissue and whole plants. We demonstrated that VACNFs penetrate the leaf surface to deliver sub-microliter quantities of solution containing fluorescent or radiolabeled molecules into Populus leaf cells. Importantly, VACNFs proved to be gentler than abrasion with carborundum, a common way to introduce material into leaves. Unlike carborundum, VACNFs did not disrupt cell or tissue integrity, nor did they induce production of hydrogen peroxide, a typical wound response. We show that femtomole to picomole quantities of labeled molecules (fluorescent dyes, small proteins and dextran), ranging from 0.5–500 kDa, can be introduced by VACNFs, and we demonstrate the use of the approach to track delivered probes from their site of introduction on the leaf to distal plant regions. VACNF arrays thus offer an attractive microdelivery method for the introduction of biomolecules and other probes into trees and potentially other types of plants. PMID:27119338

  19. Carbon Nanofiber Arrays: A Novel Tool for Microdelivery of Biomolecules to Plants.

    PubMed

    Davern, Sandra M; McKnight, Timothy E; Standaert, Robert F; Morrell-Falvey, Jennifer L; Shpak, Elena D; Kalluri, Udaya C; Jelenska, Joanna; Greenberg, Jean T; Mirzadeh, Saed

    2016-01-01

    Effective methods for delivering bioprobes into the cells of intact plants are essential for investigating diverse biological processes. Increasing research on trees, such as Populus spp., for bioenergy applications is driving the need for techniques that work well with tree species. This report introduces vertically aligned carbon nanofiber (VACNF) arrays as a new tool for microdelivery of labeled molecules to Populus leaf tissue and whole plants. We demonstrated that VACNFs penetrate the leaf surface to deliver sub-microliter quantities of solution containing fluorescent or radiolabeled molecules into Populus leaf cells. Importantly, VACNFs proved to be gentler than abrasion with carborundum, a common way to introduce material into leaves. Unlike carborundum, VACNFs did not disrupt cell or tissue integrity, nor did they induce production of hydrogen peroxide, a typical wound response. We show that femtomole to picomole quantities of labeled molecules (fluorescent dyes, small proteins and dextran), ranging from 0.5-500 kDa, can be introduced by VACNFs, and we demonstrate the use of the approach to track delivered probes from their site of introduction on the leaf to distal plant regions. VACNF arrays thus offer an attractive microdelivery method for the introduction of biomolecules and other probes into trees and potentially other types of plants. PMID:27119338

  20. Fabrication and Characterization of High Temperature Resin/Carbon Nanofiber Composites

    NASA Technical Reports Server (NTRS)

    Ghose, Sayata; Watson, Kent A.; Working, Dennis C.; Criss, Jim M.; Siochi, Emilie J.; Conell, John W.

    2005-01-01

    As part of ongoing efforts to develop multifunctional advanced composites, blends of PETI-330 and carbon nanofibers (CNF) were prepared and characterized. Dry mixing techniques were employed and the effect of CNF loading level on melt viscosity was determined. The resulting powders were characterized for degree of mixing, thermal and rheological properties. Based on the characterization results, samples containing 30 and 40 wt% CNF were scaled up to approx.300 g and used to fabricate moldings 10.2 cm x 15.2 cm x 0.32 cm thick. The moldings were fabricated by injecting the mixtures at 260-280 C into a stainless steel tool followed by curing for 1 h at 371 C. The tool was designed to impart high shear during the injection process in an attempt to achieve some alignment of CNFs in the flow direction. Moldings were obtained that were subsequently characterized for thermal, mechanical and electrical properties. The degree of dispersion and alignment of CNFs were investigated using high-resolution scanning electron microscopy. The preparation and preliminary characterization of PETI-330/CNF composites will be discussed.

  1. A Novel Carbon Nanofibers Grown on Glass Microballoons Immunosensor: A Tool for Early Diagnosis of Malaria

    PubMed Central

    Gikunoo, Emmanuel; Abera, Adeyabeba; Woldesenbet, Eyassu

    2014-01-01

    This paper presents a novel method for direct detection of Plasmodium falciparum histidine rich protein-2 (PfHRP-2) antigen using carbon nanofiber (CNF) forests grown on glass microballoons (NMBs). Secondary antibodies specific to PfHRP-2 densely attached to the CNFs exhibit extraordinary ability for the detection of minute concentrations of Plasmodium species. A sandwich immunoassay protocol was employed, where a glass substrate was used to immobilize primary antibodies at designated capture zones. High signal amplification was obtained in both colorimetric and electrical measurements due to the CNFs through specific binding. As a result, it was possible to detect PfHRP-2 levels as low as 0.025 ng/mL concentration in phosphate buffered saline (PBS) using a visual signal within only 1 min of test duration. Lower limits of 0.01 ng/mL was obtained by measuring the electrical resistivity of the capture zone. This method is also highly selective and specific in identifying PfHRP-2 and other Plasmodium species from the same solution. In addition, the stability of the labeling mechanism eliminates the false signals generated by the use of dyes in current malaria rapid diagnostic test kits (MRDTs). Thus, the rapid, sensitive and high signal amplification capabilities of NMBs is a promising tool for early diagnosis of malaria and other infectious diseases. PMID:25120159

  2. Hierarchically mesoporous CuO/carbon nanofiber coaxial shell-core nanowires for lithium ion batteries

    NASA Astrophysics Data System (ADS)

    Park, Seok-Hwan; Lee, Wan-Jin

    2015-05-01

    Hierarchically mesoporous CuO/carbon nanofiber coaxial shell-core nanowires (CuO/CNF) as anodes for lithium ion batteries were prepared by coating the Cu2(NO3)(OH)3 on the surface of conductive and elastic CNF via electrophoretic deposition (EPD), followed by thermal treatment in air. The CuO shell stacked with nanoparticles grows radially toward the CNF core, which forms hierarchically mesoporous three-dimensional (3D) coaxial shell-core structure with abundant inner spaces in nanoparticle-stacked CuO shell. The CuO shells with abundant inner spaces on the surface of CNF and high conductivity of 1D CNF increase mainly electrochemical rate capability. The CNF core with elasticity plays an important role in strongly suppressing radial volume expansion by inelastic CuO shell by offering the buffering effect. The CuO/CNF nanowires deliver an initial capacity of 1150 mAh g-1 at 100 mA g-1 and maintain a high reversible capacity of 772 mAh g-1 without showing obvious decay after 50 cycles.

  3. Three-Dimensional Force Sensing Device Using Carbon Nanofiber Polymer Composites: Design and Fabrication

    NASA Astrophysics Data System (ADS)

    Chang, Fuh-Yu; Liu, Chia-Ming; Chen, Tse-Min; Chen, Chia-Ming; Lin, Yu-Hsien; Huang, Shu-Jiuan

    2012-06-01

    We propose an innovative three-dimensional force sensing device fabricated with carbon nanofiber (CNF) polymer composites. The device has four piezoresistive strain sensors made onto a polyimide substrate using surface patterning treatment and tilted-drop process with CNF polymer solutions. The proposed design and fabrication process is simpler than that of other three-dimensional force sensors and the device is suitable for mass production. The fabricated strain sensor properties using CNF polymer solutions with different composition ratios were investigated. An equation was derived using simple percolation theory to predict the conductivity of CNF polymer composites. The measured gauge factors were in the 4.84 to 17.68 range for CNF polymer composites with CNF 8.85-45.2 wt %. A programmable system on chip (PSoC) with built-in operational (OP) amplifier, analog-to-digital (AD) converter and multiplexer was used to develop a scanning and analyzing circuit for the three-dimensional force sensing device. The proposed integrated system was successfully applied to control a computer screen cursor.

  4. Multiwalled Carbon Nanotube/nanofiber Arrays as Conductive and Dry Adhesive Interface Materials

    NASA Technical Reports Server (NTRS)

    Tong, Tao; Zhao, Yang; Delzeit, Lance; Majumdar, Arun; Kashani, Ali

    2004-01-01

    We demonstrate the possibility of making conductive and dry adhesive interfaces between multiwalled carbon nanotube (MWNT) and nanofiber (MWNF) arrays grown by chemical vapor deposition with transition-metal as catalyst on highly Boron doped silicon substrates. The maximum observed adhesion force between MWNT and MWNF surfaces is 3.5 mN for an apparent contact area of 2 mm by 4 mm. The minimum contact resistance measured at the same time is approx.20 Omega. Contact resistances of MWNT-MWNT and MWNT-gold interfaces were also measured as pressure forces around several mN were applied at the interface. The resulting minimum contact resistances are on the same order but with considerable variation from sample to sample. For MWNT-MWNT contacts, a minimum contact resistance of approx.1 Omega is observed for a contact area of 2 mm by 1 mm. The relatively high contact resistances, considering the area density of the nanotubes, might be explained by the high cross-tube resistances at the contact interfaces.

  5. Highly sensitive and selective determination of methylergometrine maleate using carbon nanofibers/silver nanoparticles composite modified carbon paste electrode.

    PubMed

    Kalambate, Pramod K; Rawool, Chaitali R; Karna, Shashi P; Srivastava, Ashwini K

    2016-12-01

    A highly sensitive and selective voltammetric method for determination of Methylergometrine maleate (MM) in pharmaceutical formulations, urine and blood serum samples has been developed based on enhanced electrochemical response of MM at carbon nanofibers and silver nanoparticles modified carbon paste electrode (CNF-AgNP-CPE). The electrode material was characterized by various techniques viz., X-ray diffraction, scanning electron microscopy and energy dispersive X-ray spectroscopy. The electrocatalytic response of MM at CNF-AgNP-CPE was studied by cyclic voltammetry (CV), differential pulse voltammetry (DPV) and electrochemical impedance spectroscopy (EIS). Under optimized conditions, the proposed sensor exhibits excellent electrochemical response towards MM. The DPV study shows greatly enhanced electrochemical signal for MM at CNF-AgNP-CPE lending high sensitivity to the proposed sensor for MM detection. The peak (Ip) current for MM is found to be rectilinear in the range 4.0×10(-8)-2.0×10(-5)M with a detection limit of 7.1×10(-9)M using DPV. The feasibility of the proposed sensor in analytical applications was investigated by conducting experiments on commercial pharmaceutical formulations, human urine and blood serum samples, which yielded satisfactory recoveries of MM. The proposed electrochemical sensor offers high sensitivity, selectivity, reproducibility and practical utility. We recommend it as an authentic and productive electrochemical sensor for successful determination of MM. PMID:27612735

  6. Adsorption of ciprofloxacin, bisphenol and 2-chlorophenol on electrospun carbon nanofibers: in comparison with powder activated carbon.

    PubMed

    Li, Xiaona; Chen, Shuo; Fan, Xinfei; Quan, Xie; Tan, Feng; Zhang, Yaobin; Gao, Jinsuo

    2015-06-01

    Carbon nanofibers (CNFs) were prepared by electrospun polyacrylonitrile (PAN) polymer solutions followed by thermal treatment. For the first time, the influence of stabilization procedure on the structure properties of CNFs was explored to improve the adsorption capacity of CNFs towards the environmental pollutants from aqueous solution. The adsorption of three organic chemicals including ciprofloxacin (CIP), bisphenol (BPA) and 2-chlorophenol (2-CP) on electrospun CNFs with high surface area of 2326m(2)/g and micro/mesoporous structure characteristics were investigated. The adsorption affinities were compared with that of the commercial powder activated carbon (PAC). The adsorption kinetics and isotherms showed that the maximum adsorption capacities (qm) of CNFs towards the three pollutants are sequenced in the order of CIP>BPA>2-CP, which are 2.6-fold (CIP), 1.6-fold (BPA) and 1.1-fold (2-CP) increase respectively in comparison with that of PAC adsorption. It was assumed that the micro/mesoporous structure of CNFs, molecular size of the pollutants and the π electron interaction play important roles on the high adsorption capacity exhibited by CNFs. In addition, electrostatic interaction and hydrophobic interaction also contribute to the adsorption of CNFs. This study demonstrates that the electrospun CNFs are promising adsorbents for the removal of pollutants from aqueous solutions. PMID:25702869

  7. Covalent immobilization of redox enzyme on electrospun nonwoven poly(acrylonitrile-co-acrylic acid) nanofiber mesh filled with carbon nanotubes: a comprehensive study.

    PubMed

    Wang, Zhen-Gang; Ke, Bei-Bei; Xu, Zhi-Kang

    2007-07-01

    In this work, novel conductive composite nanofiber mesh possessing reactive groups was electrospun from solutions containing poly(acrylonitrile-co-acrylic acid) (PANCAA) and multi-walled carbon nanotubes (MWCNTs) for redoxase immobilization, assuming that the incorporated MWCNTs could behave as electrons transferor during enzyme catalysis. The covalent immobilization of catalase from bovine liver on the neat PANCAA nanofiber mesh or the composite one was processed in the presence of EDC/NHS. Results indicated that both the amount and activity retention of bound catalase on the composite nanofiber mesh were higher than those on the neat PANCAA nanofiber mesh, and the activity increased up to 42%. Kinetic parameters, K(m) and V(max), for the catalases immobilized on the composite nanofiber mesh were lower and higher than those on the neat one, respectively. This enhanced activity might be ascribed to either promoted electron transfer through charge-transfer complexes and the pi system of carbon nanotubes or rendered biocompatibility by modified MWCNTs. Furthermore, the immobilized catalases revealed much more stability after MWCNTs were incorporated into the polymer nanofiber mesh. However, there was no significant difference in optimum pH value and temperature, thermal stability and operational stability between these two immobilized preparations, while the two ones appeared more advantageous than the free in these properties. The effect of MWCNTs incorporation on another redox enzyme, peroxidase, was also studied and it was found that the activity increased by 68% in comparison of composite one with neat preparation. PMID:17171660

  8. Utilization of porous carbons derived from coconut shell and wood in natural rubber

    Technology Transfer Automated Retrieval System (TEKTRAN)

    The porous carbons derived from cellulose are renewable and environmentally friendly. Coconut shell and wood derived porous carbons were characterized with elemental analysis, ash content, x-ray diffraction, infrared absorbance, particle size, surface area, and pore volume. The results were compared...

  9. Asphalt-derived high surface area activated porous carbons for carbon dioxide capture.

    PubMed

    Jalilov, Almaz S; Ruan, Gedeng; Hwang, Chih-Chau; Schipper, Desmond E; Tour, Josiah J; Li, Yilun; Fei, Huilong; Samuel, Errol L G; Tour, James M

    2015-01-21

    Research activity toward the development of new sorbents for carbon dioxide (CO2) capture have been increasing quickly. Despite the variety of existing materials with high surface areas and high CO2 uptake performances, the cost of the materials remains a dominant factor in slowing their industrial applications. Here we report preparation and CO2 uptake performance of microporous carbon materials synthesized from asphalt, a very inexpensive carbon source. Carbonization of asphalt with potassium hydroxide (KOH) at high temperatures (>600 °C) yields porous carbon materials (A-PC) with high surface areas of up to 2780 m(2) g(-1) and high CO2 uptake performance of 21 mmol g(-1) or 93 wt % at 30 bar and 25 °C. Furthermore, nitrogen doping and reduction with hydrogen yields active N-doped materials (A-NPC and A-rNPC) containing up to 9.3% nitrogen, making them nucleophilic porous carbons with further increase in the Brunauer-Emmett-Teller (BET) surface areas up to 2860 m(2) g(-1) for A-NPC and CO2 uptake to 26 mmol g(-1) or 114 wt % at 30 bar and 25 °C for A-rNPC. This is the highest reported CO2 uptake among the family of the activated porous carbonaceous materials. Thus, the porous carbon materials from asphalt have excellent properties for reversibly capturing CO2 at the well-head during the extraction of natural gas, a naturally occurring high pressure source of CO2. Through a pressure swing sorption process, when the asphalt-derived material is returned to 1 bar, the CO2 is released, thereby rendering a reversible capture medium that is highly efficient yet very inexpensive. PMID:25531980

  10. Cellulose nanofiber/single-walled carbon nanotube hybrid non-woven macrofiber mats as novel wearable supercapacitors with excellent stability, tailorability and reliability

    NASA Astrophysics Data System (ADS)

    Niu, Qingyuan; Gao, Kezheng; Shao, Ziqiang

    2014-03-01

    Non-woven macrofiber mats are prepared by simply controlling the extrusion patterns of cellulose nanofiber/single-walled carbon nanotube suspensions in an ethanol coagulation bath, and drying in air under restricted conditions. These novel wearable supercapacitors based on non-woven macrofiber mats are demonstrated to have excellent tailorability, electrochemical stability, and damage reliability.Non-woven macrofiber mats are prepared by simply controlling the extrusion patterns of cellulose nanofiber/single-walled carbon nanotube suspensions in an ethanol coagulation bath, and drying in air under restricted conditions. These novel wearable supercapacitors based on non-woven macrofiber mats are demonstrated to have excellent tailorability, electrochemical stability, and damage reliability. Electronic supplementary information (ESI) available: Experimental, TEM image, IR spectra, and XRD spectra of cellulose nanofibers, photograph of the cellulose nanofiber/single-walled carbon nanotube suspension, cellulose nanofiber/single-walled carbon nanotube non-woven macrofiber mat and non-woven macrofiber mat wearable supercapacitors. The electrochemical performance of the CNF/SWCNT hybrid fiber wearable supercapacitor. Photograph of the non-woven macrofiber mat wearable supercapacitors integrated within textiles. See DOI: 10.1039/c3nr05929d

  11. Study of the processes of carbonization and oxidation of porous silicon by Raman and IR spectroscopy

    SciTech Connect

    Vasin, A. V.; Okholin, P. N.; Verovsky, I. N.; Nazarov, A. N.; Lysenko, V. S.; Kholostov, K. I. Bondarenko, V. P.; Ishikawa, Y.

    2011-03-15

    Porous silicon layers were produced by electrochemical etching of single-crystal silicon wafers with the resistivity 10 {Omega} cm in the aqueous-alcohol solution of hydrofluoric acid. Raman spectroscopy and infrared absorption spectroscopy are used to study the processes of interaction of porous silicon with undiluted acetylene at low temperatures and the processes of oxidation of carbonized porous silicon by water vapors. It is established that, even at the temperature 550 Degree-Sign C, the silicon-carbon bonds are formed at the pore surface and the graphite-like carbon condensate emerges. It is shown that the carbon condensate inhibits oxidation of porous silicon by water vapors and contributes to quenching of white photoluminescence in the oxidized carbonized porous silicon nanocomposite layer.

  12. Optimized electrospinning synthesis of iron-nitrogen-carbon nanofibers for high electrocatalysis of oxygen reduction in alkaline medium

    NASA Astrophysics Data System (ADS)

    Yan, Xingxu; Liu, Kexi; Wang, Xiangqing; Wang, Tuo; Luo, Jun; Zhu, Jing

    2015-04-01

    To achieve iron-nitrogen-carbon (Fe-N-C) nanofibers with excellent electrocatalysis for replacing high-cost Pt-based catalysts in the cathodes of fuel cells and metal-air batteries, we have investigated and evaluated the effects of polyacrylonitrile (PAN) concentration and the proportion of iron to PAN, along with voltage and flow rate during the electrospinning process, and thus proposed three criteria to optimize these parameters for ideal nanofiber catalysts. The best half-wave potential of an optimized catalysts is 0.82 V versus reversible hydrogen electrode in an alkaline medium, which reaches the best range of the non-precious-metal catalysts reported and is very close to that of commercial Pt/C catalysts. Furthermore, the electron-transfer number of our catalysts is superior to that of the Pt/C, indicating the catalysts undergo a four-electron process. The durability of the optimized Fe-N-C nanofibers is also better than that of the Pt/C, which is attributed to the homogeneous distribution of the active sites in our catalysts.

  13. Optimized electrospinning synthesis of iron-nitrogen-carbon nanofibers for high electrocatalysis of oxygen reduction in alkaline medium.

    PubMed

    Yan, Xingxu; Liu, Kexi; Wang, Xiangqing; Wang, Tuo; Luo, Jun; Zhu, Jing

    2015-04-24

    To achieve iron-nitrogen-carbon (Fe-N-C) nanofibers with excellent electrocatalysis for replacing high-cost Pt-based catalysts in the cathodes of fuel cells and metal-air batteries, we have investigated and evaluated the effects of polyacrylonitrile (PAN) concentration and the proportion of iron to PAN, along with voltage and flow rate during the electrospinning process, and thus proposed three criteria to optimize these parameters for ideal nanofiber catalysts. The best half-wave potential of an optimized catalysts is 0.82 V versus reversible hydrogen electrode in an alkaline medium, which reaches the best range of the non-precious-metal catalysts reported and is very close to that of commercial Pt/C catalysts. Furthermore, the electron-transfer number of our catalysts is superior to that of the Pt/C, indicating the catalysts undergo a four-electron process. The durability of the optimized Fe-N-C nanofibers is also better than that of the Pt/C, which is attributed to the homogeneous distribution of the active sites in our catalysts. PMID:25815586

  14. Electrospun polyamide 6/poly(allylamine hydrochloride) nanofibers functionalized with carbon nanotubes for electrochemical detection of dopamine.

    PubMed

    Mercante, Luiza A; Pavinatto, Adriana; Iwaki, Leonardo E O; Scagion, Vanessa P; Zucolotto, Valtencir; Oliveira, Osvaldo N; Mattoso, Luiz H C; Correa, Daniel S

    2015-03-01

    The use of nanomaterials as an electroactive medium has improved the performance of bio/chemical sensors, particularly when synergy is reached upon combining distinct materials. In this paper, we report on a novel architecture comprising electrospun polyamide 6/poly(allylamine hydrochloride) (PA6/PAH) nanofibers functionalized with multiwalled carbon nanotubes, used to detect the neurotransmitter dopamine (DA). Miscibility of PA6 and PAH was sufficient to form a single phase material, as indicated by thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC), leading to nanofibers with no beads onto which the nanotubes could adsorb strongly. Differential pulse voltammetry was employed with indium tin oxide (ITO) electrodes coated with the functionalized nanofibers for the selective electrochemical detection of dopamine (DA), with no interference from uric acid (UA) and ascorbic acid (AA) that are normally present in biological fluids. The response was linear for a DA concentration range from 1 to 70 μmol L(-1), with detection limit of 0.15 μmol L(-1) (S/N = 3). The concepts behind the novel architecture to modify electrodes can be potentially harnessed in other electrochemical sensors and biosensors. PMID:25644325

  15. Adsorption of anionic and cationic polymers on porous and non-porous calcium carbonate surfaces

    NASA Astrophysics Data System (ADS)

    Bjorklund, Robert B.; Arwin, Hans; Järnström, Lars

    1994-01-01

    The adsorption of anionic and cationic polymers onto calcium carbonate surfaces was studied by ellipsometry. Sodium polyacrylate was observed to both adsorb on and promote dissolution of polished limestone surfaces in 5 mM CaSO 4 solution at pH 10.3. It was not possible to differentiate between the two processes when they occurred simultaneously. Cationic starch adsorbed on the limestone surfaces at low concentrations and caused mineral dissolution at higher concentrations. The adsorbed amount of starch was higher on surfaces which were first made porous by partial dissolution than on freshly polished surfaces. Surfaces created by cleavage of Iceland spar calcite were quite stable against dissolution and the amount of starch adsorbed determined by ellipsometry agreed well with the adsorbed mass determined from batch adsorption experiments on ground calcite.

  16. Nitrogen-Doped Carbon Nanocoil Array Integrated on Carbon Nanofiber Paper for Supercapacitor Electrodes.

    PubMed

    Choi, Won Ho; Choi, Mi Jin; Bang, Jin Ho

    2015-09-01

    Integrating a nanostructured carbon array on a conductive substrate remains a challenging task that presently relies primarily on high-vacuum deposition technology. To overcome the problems associated with current vacuum techniques, we demonstrate the formation of an N-doped carbon array by pyrolysis of a polymer array that was electrochemically grown on carbon fiber paper. The resulting carbon array was investigated for use as a supercapacitor electrode. In-depth surface characterization results revealed that the microtextural properties, surface functionalities, and degree of nitrogen incorporated into the N-doped carbon array can be delicately controlled by manipulating carbonization temperatures. Furthermore, electrochemical measurements showed that subtle changes in these physical properties resulted in significant changes in the capacitive behavior of the N-doped carbon array. Pore structures and nitrogen/oxygen functional groups, which are favorable for charge storage, were formed at low carbonization temperatures. This result showed the importance of having a comprehensive understanding of how the surface characteristics of carbon affect its capacitive performance. When utilized as a substrate in a pseudocapacitive electrode material, the N-doped carbon array maximizes capacitive performance by simultaneously achieving high gravimetric and areal capacitances due to its large surface area and high electrical conductivity. PMID:26264641

  17. Mineral carbonation in water-unsaturated porous media

    NASA Astrophysics Data System (ADS)

    Harrison, A. L.; Dipple, G. M.; Mayer, K. U.; Power, I. M.

    2014-12-01

    Ultramafic mine tailings have an untapped capacity to sequester CO2 directly from air or CO2-rich gas streams via carbonation of tailings minerals [1]. The CO2 sequestration capacity of these sites could be exploited simply by increasing the supply of CO2 into tailings, such as through circulation of air or flue gas from mine site power plants [1,2]. Mine tailings storage facilities typically have heterogeneously distributed pore water [1], affecting both the reactive capacity of the porous medium and the exposure of reactive phases to CO2 [3]. We examine the physical reaction processes that govern carbonation efficiency in variably saturated porous media using meter-scale column experiments containing the tailings mineral, brucite [Mg(OH)2], that were supplied with 10% CO2 gas streams. The experiments were instrumented with water content and gas phase CO2 sensors to track changes in water saturation and CO2concentration with time. The precipitation of hydrated Mg-carbonates as rinds encasing brucite particles resulted in passivation of brucite surfaces and an abrupt shut down of the reaction prior to completion. Moreover, the extent of reaction was further limited at low water saturation due to the lack of water available to form hydrated Mg-carbonates, which incorporate water into their crystal structures. Reactive transport modeling using MIN3P-DUSTY [4] revealed that the instantaneous reaction rate was not strongly affected by water saturation, but the reactive capacity was reduced significantly. Surface passivation and water-limited reaction resulted in a highly non-geometric evolution of reactive surface area. The extent of reaction was also limited at high water content because viscous fingering of the gas streams injected at the base of the columns resulted in narrow zones of highly carbonated material, but left a large proportion of brucite unreacted. The implication is that carbonation efficiency in mine tailings could be maximized by targeting an

  18. Graphene Folding in Si Rich Carbon Nanofibers for Highly Stable, High Capacity Li-Ion Battery Anodes.

    PubMed

    Fei, Ling; Williams, Brian P; Yoo, Sang H; Kim, Jangwoo; Shoorideh, Ghazal; Joo, Yong Lak

    2016-03-01

    Silicon nanoparticles (Si NPs) wrapped by graphene in carbon nanofibers were obtained via electrospinning and subsequent thermal treatment. In this study, water-soluble poly(vinyl alcohol) (PVA) with low carbon yield is selected to make the process water-based and to achieve a high silicon yield in the composite. It was also found that increasing the amount of graphene helps keep the PVA fiber morphology after carbonization, while forming a graphene network. The fiber SEM and HRTEM images reveal that micrometer graphene is heavily folded into sub-micron scale fibers during electrospinning, while Si NPs are incorporated into the folds with nanospace in between. When applied to lithium-ion battery anodes, the Si/graphene/carbon nanofiber composites show a high reversible capacity of ∼2300 mAh g(-1) at a charging rate of 100 mA/g and a stable capacity of 1191 mAh g(-1) at 1 A/g after more than 200 cycles. The interconnected graphene network not only ensures the excellent conductivity but also serves as a buffering matrix for the mechanic stress caused by volume change; the nanospace between Si NPs and folded graphene provides the space needed for volume expansion. PMID:26853163

  19. Bicontinuous Structure of Li₃V₂(PO₄)₃ Clustered via Carbon Nanofiber as High-Performance Cathode Material of Li-Ion Batteries.

    PubMed

    Chen, Lin; Yan, Bo; Xu, Jing; Wang, Chunguang; Chao, Yimin; Jiang, Xuefan; Yang, Gang

    2015-07-01

    In this work, the composite structure of Li3V2(PO4)3 (LVP) nanoparticles with carbon nanofibers (CNF) is designed. The size and location of LVP particles, and the degree of graphitization and diameter of carbon nanofibers, are optimized by electrospinning and heat treatment. The bicontinuous morphologies of LVP/CNF are dependent on the carbonization of PVP and simultaneous growing of LVP, with the fibers shrunk and the LVP crystals grown toward the outside. LVP nanocystals clustered via carbon nanofibers guarantee improving the diffusion ability of Li(+), and the carbon fiber simultaneously guarantees the effective electron conductivity. Compared with the simple carbon-coated LVP and pure LVP, the particle-clustered structure guarantees high rate capability and long-life cycling stability of NF-LVP as cathode for LIBs. At 20 C rate in the range 3.0-4.3 V, NF-LVP delivers the initial capacity of 122.6 mAh g(-1) close to the theoretical value of 133 mAh g(-1), and maintains 97% of the initial capacity at the 1000th cycle. The bead-like structure of cathode material clustered via carbon nanofibers via electrospinning will be further applied to high-performance LIBs. PMID:26053376

  20. Revealing the Role of Catalysts in Carbon Nanotubes and Nanofibers by Scanning Transmission X-ray Microscopy

    PubMed Central

    Gao, Jing; Zhong, Jun; Bai, Lili; Liu, Jinyin; Zhao, Guanqi; Sun, Xuhui

    2014-01-01

    The identification of effective components on the atomic scale in carbon nanomaterials which improve the performance in various applications remains outstanding challenges. Here the catalyst residues in individual carbon nanotube (CNT) and carbon nanofiber (CNF) were clearly imaged with a concurrent characterization of their electronic structure by nanoscale scanning transmission X-ray microscopy. Except for prominent catalyst nanoparticle at the tip, tiny catalyst clusters along the tube (fiber) were detected, indicating a migration of the catalysts with the growth of CNTs (CNFs). The observation provides the direct evidence on the atomic metal in CNT for oxygen reduction reported in the literature. Interaction between catalysts (Fe, Ni) and CNTs (CNFs) at the tip was also identified by comparing the X-ray absorption spectra. A deep understanding of catalyst residues such as Fe or Ni in carbon nanomaterials is very vital to growth mechanism development and practical applications. PMID:24398972

  1. Microfluidic production of porous carbon spheres with tunable size and pores.

    PubMed

    Ge, Han; Xu, Hongbao; Lu, Tianyi; Li, Jiang; Chen, Haosheng; Wan, Jiandi

    2016-01-01

    Porous carbon particles have been widely used in many areas including energy storage. Production of carbon microspheres in an efficient, controlled, and low-cost manner, however, is challenging. Here, we demonstrate a microfluidic approach to generate porous carbon particles using inexpensive precursors and show that the size of the particle and pores can be tuned by adjusting the deionized (DI) water content in droplets and preheating temperature. The developed strategy offers an effective approach to control the production of porous carbon spheres with a well-defined diameter, narrow size distribution and pore size. PMID:26397924

  2. Mobility of Multi-walled Carbon Nanotubes in Porous Media

    NASA Astrophysics Data System (ADS)

    O'Carroll, D. M.; Liu, X.; Petersen, E.; Huang, Q.; Anderson, L.

    2007-12-01

    Engineered multi-walled carbon nanotubes (MWCNTs) are the subject of intense research and are expected to gain widespread usage in a broad variety of commercial products. However concerns have been raised regarding their potential environmental and health risks. The mobility of MWCNTs in porous media is examined in this study through one dimensional flow-through column experiments under conditions representative of subsurface and drinking water treatment systems. The goal of this work was to determine dominant MWCNT removal mechanisms and factors that control MWCNT transport. Results demonstrate that pore water velocity strongly influenced MWCNT transport, a result that stands in contrast to traditional colloid filtration theory, which suggests a relatively minor effect of flow velocity in comparison to Brownian diffusion. Experiments conducted at different ionic strengths indicate that both particle deposition and straining are important MWCNT removal mechanisms from the aqueous phase. Given these findings, traditional colloid filtration theory may not be appropriate for the prediction of MWCNT mobility in porous media. This may be due to the large aspect ratio of the MWCNTs and the importance of straining in MWCNT removal.

  3. Monolithic porous graphitic carbons obtained through catalytic graphitization of carbon xerogels

    NASA Astrophysics Data System (ADS)

    Kiciński, Wojciech; Norek, Małgorzata; Bystrzejewski, Michał

    2013-01-01

    Pyrolysis of organic xerogels accompanied by catalytic graphitization and followed by selective-combustion purification was used to produce porous graphitic carbons. Organic gels impregnated with iron(III) chloride or nickel(II) acetate were obtained through polymerization of resorcinol and furfural. During the pyrolysis stage graphitization of the gel matrix occurs, which in turn develops mesoporosity of the obtained carbons. The evolution of the carbon into graphitic structures is strongly dependent on the concentrations of the transition metal. Pyrolysis leads to monoliths of carbon xerogel characterized by substantially enhanced mesoporosity resulting in specific surface areas up to 400 m2/g. Removal of the amorphous carbon by selective-combustion purification reduces the xerogels' mesoporosity, occasionally causing loss of their mechanical strength. The graphitized carbon xerogels were investigated by means of SEM, XRD, Raman scattering, TG-DTA and N2 physisorption. Through this procedure well graphitized carbonaceous materials can be obtained as bulk pieces.

  4. Rational Design of Efficient Electrocatalysts for Hydrogen Evolution Reaction: Single Layers of WS2 Nanoplates Anchored to Hollow Nitrogen-Doped Carbon Nanofibers.

    PubMed

    Yu, Sunmoon; Kim, Jaehoon; Yoon, Ki Ro; Jung, Ji-Won; Oh, Jihun; Kim, Il-Doo

    2015-12-30

    To exploit the benefits of nanostructuring for enhanced hydrogen evolution reaction (HER), we employed coaxial electrospinning to synthesize single-layered WS2 nanoplates anchored to hollow nitrogen-doped carbon nanofibers (WS2@HNCNFs) as efficient electrocatalysts. For comparison, bulk WS2 powder and single layers of WS2 embedded in nitrogen-doped carbon nanofibers (WS2@NCNFs) were synthesized and electrochemically tested. The distinctive design of the WS2@HNCNFs enables remarkable electrochemical performances showing a low overpotential with reduced charge transfer resistance, a small Tafel slope, and excellent durability. The experimental results highlight the importance of nanostructure engineering in electrocatalysts for enhanced HER. PMID:26654256

  5. Stainless steel mesh supported nitrogen-doped carbon nanofibers for binder-free cathode in microbial fuel cells.

    PubMed

    Chen, Shuiliang; Chen, Yu; He, Guanghua; He, Shuijian; Schröder, Uwe; Hou, Haoqing

    2012-04-15

    In this communication, we report a binder-free oxygen reduction cathode for microbial fuel cells. The binder-free cathode is prepared by growth of nitrogen-doped carbon nanofibers (NCNFs) on stainless steel mesh (SSM) via simple pyrolysis of pyridine. The interaction force between NCNFs and SSM surface is very strong which is able to tolerate water flush. The NCNFs/SSM cathode shows high and stable electrocatalytic activity for oxygen reduction reaction, which is comparable to that of Pt/SSM and ferricyanide cathode. This study proposes a promising low-cost binder-free cathode for microbial fuel cells. PMID:22336437

  6. A Precision Dose Control Circuit for Maskless E-Beam Lithography With Massively Parallel Vertically Aligned Carbon Nanofibers

    SciTech Connect

    Eliza, Sazia A.; Islam, Syed K; Rahman, Touhidur; Bull, Nora D; Blalock, Benjamin; Baylor, Larry R; Ericson, Milton Nance; Gardner, Walter L

    2011-01-01

    This paper describes a highly accurate dose control circuit (DCC) for the emission of a desired number of electrons from vertically aligned carbon nanofibers (VACNFs) in a massively parallel maskless e-beam lithography system. The parasitic components within the VACNF device cause a premature termination of the electron emission, resulting in underexposure of the photoresist. In this paper, we compensate for the effects of the parasitic components and noise while reducing the area of the chip and achieving a precise count of emitted electrons from the VACNFs to obtain the optimum dose for the e-beam lithography.

  7. Pumpkin-Derived Porous Carbon for Supercapacitors with High Performance.

    PubMed

    Bai, Suying; Tan, Guangqun; Li, Xiaoqin; Zhao, Qian; Meng, Yan; Wang, Yujue; Zhang, Yongzhi; Xiao, Dan

    2016-06-21

    Pumpkin has been employed for the first time as a renewable, low-cost precursor for the preparation of porous carbon materials with excellent performance. Unlike most other precursors, pumpkin is rich in sugars and starch, and it has advantageous properties for large-scale production. The as-prepared materials adopted a unique morphology that consisted of numerous fused sphere-like carbon grains with a high specific surface area (2968 m(2)  g(-1) ), abundant micro and mesopores, and excellent electrochemical properties. The pumpkin-derived activated carbon (PAC) material not only exhibited a high specific capacitance of 419 F g(-1) , but also showed considerable cycling stability, with 93.6 % retention after 10 000 cycles. Moreover, a symmetrical supercapacitor that was based on PAC showed a high energy density of 22.1 W h kg(-1) in aqueous electrolyte. These superior properties demonstrate that PAC holds great promise for applications in electrochemical energy-storage devices. PMID:27124360

  8. Porous three-dimensional carbon nanotube scaffolds for tissue engineering.

    PubMed

    Lalwani, Gaurav; Gopalan, Anu; D'Agati, Michael; Sankaran, Jeyantt Srinivas; Judex, Stefan; Qin, Yi-Xian; Sitharaman, Balaji

    2015-10-01

    Assembly of carbon nanomaterials into three-dimensional (3D) architectures is necessary to harness their unique physiochemical properties for tissue engineering and regenerative medicine applications. Herein, we report the fabrication and comprehensive cytocompatibility assessment of 3D chemically crosslinked macrosized (5-8 mm height and 4-6 mm diameter) porous carbon nanotube (CNT) scaffolds. Scaffolds prepared via radical initiated thermal crosslinking of single- or multiwalled CNTs (SWCNTs and MWCNTs) possess high porosity (>80%), and nano-, micro-, and macroscale interconnected pores. MC3T3 preosteoblast cells on MWCNT and SWCNT scaffolds showed good cell viability comparable to poly(lactic-co-glycolic) acid (PLGA) scaffolds after 5 days. Confocal live cell and immunofluorescence imaging showed that MC3T3 cells were metabolically active and could attach, proliferate, and infiltrate MWCNT and SWCNT scaffolds. SEM imaging corroborated cell attachment and spreading and suggested that cell morphology is governed by scaffold surface roughness. MC3T3 cells were elongated on scaffolds with high surface roughness (MWCNTs) and rounded on scaffolds with low surface roughness (SWCNTs). The surface roughness of scaffolds may be exploited to control cellular morphology and, in turn, govern cell fate. These results indicate that crosslinked MWCNTs and SWCNTs scaffolds are cytocompatible, and open avenues toward development of multifunctional all-carbon scaffolds for tissue engineering applications. PMID:25788440

  9. Asymmetric capacitors using lignin-based hierarchical porous carbons

    NASA Astrophysics Data System (ADS)

    Salinas-Torres, David; Ruiz-Rosas, Ramiro; Valero-Romero, María José; Rodríguez-Mirasol, José; Cordero, Tomás; Morallón, Emilia; Cazorla-Amorós, Diego

    2016-09-01

    Hierarchical porous carbons (HPC) were fabricated from lignin by hard template method using Beta and Y zeolites as templates. Textural properties were dictated by the hard template, obtaining a bi-modal pore size distribution with similar micropore sizes but different mesopore sizes. These HPCs provide a well-connected and developed porosity that show capacitance values near to 140 F g-1 in 1 M H2SO4 at 1 A g-1 and a capacitance retention of ca. 50% and 40% when the specific current is increased from 1 to 64 A g-1 for the Y and the Beta-based carbons, respectively. A symmetric capacitor working at 1.2 V with energy densities of 4.2 Wh kg-1 at 1.3 kW kg-1 has been obtained using the Beta-based HPC. Asymmetric in mass design allowed to operate the capacitor safely at 1.4 V, yielding an energy density of 6.3 Wh kg-1 at 1.3 kW kg-1, an increase of 50% with respect to the symmetric configuration, while keeping a maximum power near to 50 kW kg-1. This capacitor has an energy density comparable to that of a symmetric supercapacitor built using a commercial activated carbon of much higher porosity development, outperforming it in terms of energy, coulombic efficiencies and maximum power.

  10. Carbon nanofiber reinforced epoxy matrix composites and syntactic foams - mechanical, thermal, and electrical properties

    NASA Astrophysics Data System (ADS)

    Poveda, Ronald Leonel

    The tailorability of composite materials is crucial for use in a wide array of real-world applications, which range from heat-sensitive computer components to fuselage reinforcement on commercial aircraft. The mechanical, electrical, and thermal properties of composites are highly dependent on their material composition, method of fabrication, inclusion orientation, and constituent percentages. The focus of this work is to explore carbon nanofibers (CNFs) as potential nanoscale reinforcement for hollow particle filled polymer composites referred to as syntactic foams. In the present study, polymer composites with high weight fractions of CNFs, ranging from 1-10 wt.%, are used for quasi-static and high strain rate compression analysis, as well as for evaluation and characterization of thermal and electrical properties. It is shown that during compressive characterization of vapor grown carbon nanofiber (CNF)/epoxy composites in the strain rate range of 10-4-2800 s-1, a difference in the fiber failure mechanism is identified based on the strain rate. Results from compression analyses show that the addition of fractions of CNFs and glass microballoons varies the compressive strength and elastic modulus of epoxy composites by as much as 53.6% and 39.9%. The compressive strength and modulus of the syntactic foams is also shown to generally increase by a factor of 3.41 and 2.96, respectively, with increasing strain rate when quasi-static and high strain rate testing data are compared, proving strain rate sensitivity of these reinforced composites. Exposure to moisture over a 6 month period of time is found to reduce the quasi-static and high strain rate strength and modulus, with a maximum of 7% weight gain with select grades of CNF/syntactic foam. The degradation of glass microballoons due to dealkalization is found to be the primary mechanism for reduced mechanical properties, as well as moisture diffusion and weight gain. In terms of thermal analysis results, the

  11. Higher-power supercapacitor electrodes based on mesoporous manganese oxide coating on vertically aligned carbon nanofibers

    NASA Astrophysics Data System (ADS)

    Klankowski, Steven A.; Pandey, Gaind P.; Malek, Gary; Thomas, Conor R.; Bernasek, Steven L.; Wu, Judy; Li, Jun

    2015-04-01

    A study on the development of high-power supercapacitor materials based on formation of thick mesoporous MnO2 shells on a highly conductive 3D template using vertically aligned carbon nanofibers (VACNFs). Coaxial manganese shells of 100 to 600 nm nominal thicknesses are sputter-coated on VACNFs and then electrochemically oxidized into rose-petal-like mesoporous MnO2 structure. Such a 3D MnO2/VACNF hybrid architecture provides enhanced ion diffusion throughout the whole MnO2 shell and yields excellent current collection capability through the VACNF electrode. These two effects collectively enable faster electrochemical reactions during charge-discharge of MnO2 in 1 M Na2SO4. Thick MnO2 shells (up to 200 nm in radial thickness) can be employed, giving a specific capacitance up to 437 F g-1. More importantly, supercapacitors employing such a 3D MnO2/VACNF hybrid electrode illustrate more than one order of magnitude higher specific power than the state-of-the-art ones based on other MnO2 structures, reaching ~240 kW kg-1, while maintaining a comparable specific energy in the range of 1 to 10 Wh kg-1. This hybrid approach demonstrates the potential of 3D core-shell architectures for high-power energy storage devices.A study on the development of high-power supercapacitor materials based on formation of thick mesoporous MnO2 shells on a highly conductive 3D template using vertically aligned carbon nanofibers (VACNFs). Coaxial manganese shells of 100 to 600 nm nominal thicknesses are sputter-coated on VACNFs and then electrochemically oxidized into rose-petal-like mesoporous MnO2 structure. Such a 3D MnO2/VACNF hybrid architecture provides enhanced ion diffusion throughout the whole MnO2 shell and yields excellent current collection capability through the VACNF electrode. These two effects collectively enable faster electrochemical reactions during charge-discharge of MnO2 in 1 M Na2SO4. Thick MnO2 shells (up to 200 nm in radial thickness) can be employed, giving a

  12. Fe2O3 nanorods/carbon nanofibers composite: Preparation and performance as anode of high rate lithium ion battery

    NASA Astrophysics Data System (ADS)

    Wu, Chunyu; Li, Xiaoping; Li, Weishan; Li, Bin; Wang, Yaqiong; Wang, Yating; Xu, Mengqing; Xing, Lidan

    2014-04-01

    A novel Fe2O3/carbon composite is prepared using a facile one-step hydrothermal method. Its structure, morphology and performance as anode of lithium ion battery are investigated with X-ray diffraction, scanning electron microscopy, thermogravimetry, cyclic voltammetry, galvanostatic charge/discharge, and electrochemical impedance spectroscopy. It is found that the as-prepared composite is composed of α-Fe2O3 nanorods of about 75 nm in diameter and 1 μm in length, which are enwrapped with soft and curly carbon nanofibers, and exhibits superior charge/discharge performance compared to bare α-Fe2O3 nanorods, especially at high current rate. The discharge capacity is 1069 mAh g-1 at the first cycle and remains 560 mAh g-1 after 30 cycles at 0.2C for the bare nanorods, but improved to 1278 mAh g-1 and 960 mAh g-1 for the composite. At 12C, the discharge capacity is only 798 mAh g-1 initially and becomes 98 mAh g-1 after 30 cycles for the bare nanorods, while 844 mAh g-1 and 292 mAh g-1 for the composite. The improved performance of the composite is attributed to the bondage from carbon nanofibers, which contributes to the improvement in electronic conductivity and structure stability of α-Fe2O3 nanorods.

  13. Carbon Nanotube and Nanofiber Exposure Assessments: An Analysis of 14 Site Visits.

    PubMed

    Dahm, Matthew M; Schubauer-Berigan, Mary K; Evans, Douglas E; Birch, M Eileen; Fernback, Joseph E; Deddens, James A

    2015-07-01

    Recent evidence has suggested the potential for wide-ranging health effects that could result from exposure to carbon nanotubes (CNT) and carbon nanofibers (CNF). In response, the National Institute for Occupational Safety and Health (NIOSH) set a recommended exposure limit (REL) for CNT and CNF: 1 µg m(-3) as an 8-h time weighted average (TWA) of elemental carbon (EC) for the respirable size fraction. The purpose of this study was to conduct an industrywide exposure assessment among US CNT and CNF manufacturers and users. Fourteen total sites were visited to assess exposures to CNT (13 sites) and CNF (1 site). Personal breathing zone (PBZ) and area samples were collected for both the inhalable and respirable mass concentration of EC, using NIOSH Method 5040. Inhalable PBZ samples were collected at nine sites while at the remaining five sites both respirable and inhalable PBZ samples were collected side-by-side. Transmission electron microscopy (TEM) PBZ and area samples were also collected at the inhalable size fraction and analyzed to quantify and size CNT and CNF agglomerate and fibrous exposures. Respirable EC PBZ concentrations ranged from 0.02 to 2.94 µg m(-3) with a geometric mean (GM) of 0.34 µg m(-3) and an 8-h TWA of 0.16 µg m(-3). PBZ samples at the inhalable size fraction for EC ranged from 0.01 to 79.57 µg m(-3) with a GM of 1.21 µg m(-3). PBZ samples analyzed by TEM showed concentrations ranging from 0.0001 to 1.613 CNT or CNF-structures per cm(3) with a GM of 0.008 and an 8-h TWA concentration of 0.003. The most common CNT structure sizes were found to be larger agglomerates in the 2-5 µm range as well as agglomerates >5 µm. A statistically significant correlation was observed between the inhalable samples for the mass of EC and structure counts by TEM (Spearman ρ = 0.39, P < 0.0001). Overall, EC PBZ and area TWA samples were below the NIOSH REL (96% were <1 μg m(-3) at the respirable size fraction), while 30% of the inhalable PBZ EC

  14. Carbon Nanotube and Nanofiber Exposure Assessments: An Analysis of 14 Site Visits

    PubMed Central

    Dahm, Matthew M.; Schubauer-Berigan, Mary K.; Evans, Douglas E.; Birch, M. Eileen; Fernback, Joseph E.; Deddens, James A.

    2015-01-01

    Recent evidence has suggested the potential for wide-ranging health effects that could result from exposure to carbon nanotubes (CNT) and carbon nanofibers (CNF). In response, the National Institute for Occupational Safety and Health (NIOSH) set a recommended exposure limit (REL) for CNT and CNF: 1 µg m−3 as an 8-h time weighted average (TWA) of elemental carbon (EC) for the respirable size fraction. The purpose of this study was to conduct an industrywide exposure assessment among US CNT and CNF manufacturers and users. Fourteen total sites were visited to assess exposures to CNT (13 sites) and CNF (1 site). Personal breathing zone (PBZ) and area samples were collected for both the inhalable and respirable mass concentration of EC, using NIOSH Method 5040. Inhalable PBZ samples were collected at nine sites while at the remaining five sites both respirable and inhalable PBZ samples were collected side-by-side. Transmission electron microscopy (TEM) PBZ and area samples were also collected at the inhalable size fraction and analyzed to quantify and size CNT and CNF agglomerate and fibrous exposures. Respirable EC PBZ concentrations ranged from 0.02 to 2.94 µg m−3 with a geometric mean (GM) of 0.34 µg m−3 and an 8-h TWA of 0.16 µg m−3. PBZ samples at the inhalable size fraction for EC ranged from 0.01 to 79.57 µg m−3 with a GM of 1.21 µg m−3. PBZ samples analyzed by TEM showed concentrations ranging from 0.0001 to 1.613 CNT or CNF-structures per cm3 with a GM of 0.008 and an 8-h TWA concentration of 0.003. The most common CNT structure sizes were found to be larger agglomerates in the 2–5 µm range as well as agglomerates >5 µm. A statistically significant correlation was observed between the inhalable samples for the mass of EC and structure counts by TEM (Spearman ρ = 0.39, P < 0.0001). Overall, EC PBZ and area TWA samples were below the NIOSH REL (96% were <1 μg m−3 at the respirable size fraction), while 30% of the inhalable PBZ EC

  15. Greater cardiomyocyte density on aligned compared with random carbon nanofibers in polymer composites.

    PubMed

    Asiri, Abdullah M; Marwani, Hadi M; Khan, Sher Bahadar; Webster, Thomas J

    2014-01-01

    Carbon nanofibers (CNFs) randomly embedded in poly (lactic-co-glycolic-acid) (PLGA) composites have recently been shown to promote cardiomyocyte growth when compared with conventional PLGA without CNFs. It was shown then that PLGA:CNF composites were conductive and that conductivity increased as greater amounts of CNFs were added to pure PLGA. Moreover, tensile tests showed that addition of CNFs increased the tensile strength of the PLGA composite to mimic that of natural heart tissue. Most importantly, throughout all cytocompatibility experiments, cardiomyocytes were viable and expressed important biomarkers that were greatest on 50:50 wt% CNF:PLGA composites. The increased selective adsorption of fibronectin and vitronectin (critical proteins that mediate cardiomyocyte function) onto such composites proved to be the mechanism of action. However, the natural myocardium is anisotropic in terms of mechanical and electrical properties, which was not emulated in these prior PLGA:CNF composites. Thus, the aim of this in vitro study was to create and characterize CNFs aligned in PLGA composites (at 50:50 wt%, including their mechanical and electrical properties and cardiomyocyte density), comparing such results with randomly oriented CNFs in PLGA. Specifically, CNFs were added to soluble biodegradable PLGA (50:50 PGA:PLA weight ratio) and aligned by applying a voltage and then allowing the polymer to cure. CNF surface micron patterns (20 μm wide) on PLGA were then fabricated through a mold method to further mimic myocardium anisotropy. The results demonstrated anisotropic mechanical and electrical properties and significantly improved cardiomyocyte density for up to 5 days on CNFs aligned in PLGA compared with being randomly oriented in PLGA. These results indicate that CNFs aligned in PLGA should be further explored for improving cardiomyocyte density, which is necessary in numerous cardiovascular applications. PMID:25489241

  16. An amperometric uric acid biosensor based on chitosan-carbon nanotubes electrospun nanofiber on silver nanoparticles.

    PubMed

    Numnuam, Apon; Thavarungkul, Panote; Kanatharana, Proespichaya

    2014-06-01

    A novel amperometric uric acid biosensor was fabricated by immobilizing uricase on an electrospun nanocomposite of chitosan-carbon nanotubes nanofiber (Chi-CNTsNF) covering an electrodeposited layer of silver nanoparticles (AgNPs) on a gold electrode (uricase/Chi-CNTsNF/AgNPs/Au). The uric acid response was determined at an optimum applied potential of -0.35 V vs Ag/AgCl in a flow-injection system based on the change of the reduction current for dissolved oxygen during oxidation of uric acid by the immobilized uricase. The response was directly proportional to the uric acid concentration. Under the optimum conditions, the fabricated uric acid biosensor had a very wide linear range, 1.0-400 μmol L(-1), with a very low limit of detection of 1.0 μmol L(-1) (s/n = 3). The operational stability of the uricase/Chi-CNTsNF/AgNPs/Au biosensor (up to 205 injections) was excellent and the storage life was more than six weeks. A low Michaelis-Menten constant of 0.21 mmol L(-1) indicated that the immobilized uricase had high affinity for uric acid. The presence of potential common interfering substances, for example ascorbic acid, glucose, and lactic acid, had negligible effects on the performance of the biosensor. When used for analysis of uric acid in serum samples, the results agreed well with those obtained by use of the standard enzymatic colorimetric method (P > 0.05). PMID:24718436

  17. Aerosol Monitoring during Carbon Nanofiber Production: Mobile Direct-Reading Sampling

    PubMed Central

    Evans, Douglas E.; Ku, Bon Ki; Birch, M. Eileen; Dunn, Kevin H.

    2010-01-01

    Detailed investigations were conducted at a facility that manufactures and processes carbon nanofibers (CNFs). Presented research summarizes the direct-reading monitoring aspects of the study. A mobile aerosol sampling platform, equipped with an aerosol instrument array, was used to characterize emissions at different locations within the facility. Particle number, respirable mass, active surface area, and photoelectric response were monitored with a condensation particle counter (CPC), a photometer, a diffusion charger, and a photoelectric aerosol sensor, respectively. CO and CO2 were additionally monitored. Combined simultaneous monitoring of these metrics can be utilized to determine source and relative contribution of airborne particles (CNFs and others) within a workplace. Elevated particle number concentrations, up to 1.15 × 106 cm−3, were found within the facility but were not due to CNFs. Ultrafine particle emissions, released during thermal treatment of CNFs, were primarily responsible. In contrast, transient increases in respirable particle mass concentration, with a maximum of 1.1 mg m−3, were due to CNF release through uncontrolled transfer and bagging. Of the applied metrics, our findings suggest that particle mass was probably the most useful and practical metric for monitoring CNF emissions in this facility. Through chemical means, CNFs may be selectively distinguished from other workplace contaminants (Birch et al., in preparation), and for direct-reading monitoring applications, the photometer was found to provide a reasonable estimate of respirable CNF mass concentration. Particle size distribution measurements were conducted with an electrical low-pressure impactor and a fast particle size spectrometer. Results suggest that the dominant CNF mode by particle number lies between 200 and 250 nm for both aerodynamic and mobility equivalent diameters. Significant emissions of CO were also evident in this facility. Exposure control recommendations

  18. Facilitated transport channels in carbon nanotube/carbon nanofiber hierarchical composites decorated with manganese dioxide for flexible supercapacitors

    NASA Astrophysics Data System (ADS)

    Wang, Tao; Song, Dengfei; Zhao, Hao; Chen, Jiayi; Zhao, Changhui; Chen, Lulu; Chen, Wanjun; Zhou, Jinyuan; Xie, Erqing

    2015-01-01

    Freestanding carbon nanotube/carbon nanofiber (CNT/CNF) composites are prepared using electrospun CNFs as skeletons in a tubular chemical vapor deposition system. The obtained CNT/CNF composites show a hierarchical structure with a high special surface area, a high conductance (1250 S cm-1 for a 10 mm × 20 mm sample), and a high flexibility. After coated with manganese dioxide (MnO2) via an in-situ redox deposition for 0.5 h (∼0.33 mg), the CNT/CNF/MnO2 electrodes show a high specific capacitance of 517 F g-1 at a scan rate of 5 mV s-1, which is about 5.6 time higher than that CNF/MnO2-0.25 h ones with MnO2 of ∼0.36 mg. Moreover, this CNT/CNF/MnO2 electrodes show a much higher rate capability (57% at current density of 14 A g-1) than CNF/MnO2 ones (24% at 14 A g-1), and also show a higher cycling stability (maintaining 75% of the initial capacitance at cycle number of 1000). In addition, the symmetric supercapacitor assembled using two piece CNT/CNF/MnO2 electrodes shows their maximum energy density of 3.88 Wh kg-1 at power density of 7000 W kg-1. The capacitance of the assembled capacitor maintains 70% after 100 bending cycles, indicating a good flexibility. These enhancements in EC performances should be due to our designed hierarchical structures. It is suggested that such freestanding flexible CNFs/CNTs/MnO2 hierarchical composites are highly promising for high-performance flexible supercapacitors.

  19. Fabrication of carbon nanofiber-reinforced aluminum matrix composites assisted by aluminum coating formed on nanofiber surface by in situ chemical vapor deposition

    NASA Astrophysics Data System (ADS)

    Ogawa, Fumio; Masuda, Chitoshi

    2015-01-01

    The van der Waals agglomeration of carbon nanofibers (CNFs) and the weight difference and poor wettability between CNFs and aluminum hinder the fabrication of dense CNF-reinforced aluminum matrix composites with superior properties. In this study, to improve this situation, CNFs were coated with aluminum by a simple and low-cost in situ chemical vapor deposition (in situ CVD). Iodine was used to accelerate the transport of aluminum atoms. The coating layer formed by the in situ CVD was characterized using scanning electron microscopy, transmission electron microscopy, x-ray diffraction, Fourier transform-infrared spectroscopy, and x-ray photoelectron spectroscopy. The results confirmed that the CNFs were successfully coated with aluminum. The composites were fabricated to investigate the effect of the aluminum coating formed on the CNFs. The dispersion of CNFs, density, Vickers micro-hardness and thermal conductivity of the composites fabricated by powder metallurgy were improved. Pressure-less infiltration experiments were conducted to fabricate composites by casting. The results demonstrated that the wettability and infiltration were dramatically improved by the aluminum coating layer on CNFs. The aluminum coating formed by the in situ CVD technique was proved to be effective for the fabrication of CNF-reinforced aluminum matrix composites.

  20. High-yield harvest of nanofibers/mesoporous carbon composite by pyrolysis of waste biomass and its application for high durability electrochemical energy storage.

    PubMed

    Liu, Wu-Jun; Tian, Ke; He, Yan-Rong; Jiang, Hong; Yu, Han-Qing

    2014-12-01

    Disposal and recycling of the large scale biomass waste is of great concern. Themochemically converting the waste biomass to functional carbon nanomaterials and bio-oil is an environmentally friendly apporach by reducing greenhouse gas emissions and air pollution caused by open burning. In this work, we reported a scalable, "green" method for the synthesis of the nanofibers/mesoporous carbon composites through pyrolysis of the Fe(III)-preloaded biomass, which is controllable by adjustment of temperature and additive of catalyst. It is found that the coupled catalytic action of both Fe and Cl species is able to effectively catalyze the growth of the carbon nanofibers on the mesoporous carbon and form magnetic nanofibers/mesoporous carbon composites (M-NMCCs). The mechanism for the growth of the nanofibers is proposed as an in situ vapor deposition process, and confirmed by the XRD and SEM results. M-NMCCs can be directly used as electrode materials for electrochemical energy storage without further separation, and exhibit favorable energy storage performance with high EDLC capacitance, good retention capability, and excellent stability and durability (more than 98% capacitance retention after 10,000 cycles). Considering that biomass is a naturally abundant and renewable resource (over billions tons biomass produced every year globally) and pyrolysis is a proven technique, M-NMCCs can be easily produced at large scale and become a sustainable and reliable resource for clean energy storage. PMID:25372400

  1. A structural study and magnetic properties of electrospun carbon/manganese ferrite (C/MnFe2O4) composite nanofibers

    NASA Astrophysics Data System (ADS)

    Kidkhunthod, Pinit; Nilmoung, Sukanya; Mahakot, Sompin; Rodporn, Somboonsub; Phumying, Santi; Maensiri, Santi

    2016-03-01

    Carbon/manganese ferrite (C/MnFe2O4) composite nanofibers were fabricated using electrospinning technique followed by carbonization process under mixed of air and argon atmosphere at 400, 600 and 800 °C, respectively. The prepared composite nanofibers were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), vibrating sample magnetometry (VSM) and X-ray absorption spectroscopy (XAS) including X-ray absorption near edge structure (XANES) and extended X-ray absorption fine structure (EXAFS). After calcination at 800 °C, the composite nanofibers of C/MnFe2O4 were obtained with a mean diameter of nanofibers of approximately 700-800 nm. The structure of MnFe2O4 was successfully studied using XAS technique and was found to be cubic spinel with a coupling of Mn2/Mn3+ and Fe3+ oxidation states. All composite nanofibers exhibited ferromagnetic behavior especially after being calcined at 800 °C. This ferromagnetic properties were related to the distribution of cations over tetrahedral and octahedral sites as revealed by EXAFS results.

  2. Supercritical adsorption testing of porous silicon, activated carbon, and zeolite materials

    NASA Astrophysics Data System (ADS)

    Harvey, Brendan

    The supercritical adsorption of methane gas on porous silicon, activated carbon, and zeolite materials was studied. An apparatus that utilizes the volumetric adsorption measurement technique was designed and constructed to conduct the experiments. Activated carbon materials consisted of Norit RX3 Extra, Zorflex FM30K woven activated carbon cloth, and Zorflex FM10 knitted activated carbon cloth. Zeolite materials consisted of 3A, 4A, 5A, and 13X zeolites. Porous silicon materials consisted of stain etched and electrochemically etched porous films, and stain etched porous powder. All adsorption tests were conducted at room temperature (approximately 298 K) and pressures up to approximately 5 MPa. Overall, the Norit RX3 Extra granulated activated carbon produced the highest excess adsorption and effective storage capacities. Effective storage and delivery capacities of 109 and 90 stpmlml were obtained at a pressure of 3.5 MPa and a temperature of approximately 298 K.

  3. Growth and Characterization of Carbon Nanofibers on Fe/C-Fiber Textiles Coated by Deposition-Precipitation and Dip-Coating.

    PubMed

    Lee, Sang-Won; Lee, Chang-Seop

    2015-09-01

    This research was conducted to synthesize carbon nanofibers on C-fiber textiles, by thermal chemical vapor deposition (CVD) using Fe catalyst. The substrate, which was a carbon textile consisting of non-woven carbon fibers and attached graphite particles, was oxidized by nitric acid, before the deposition process. Hydroxyl groups were created on the C-fiber textile, due to the oxidization step. Fe(III) hydroxide was subsequently deposited on the oxidized surface of the C-fiber textile. To deposit ferric particles, two different methods were tested: (i) deposition-precipitation, and (ii) dip-coating. For the experiments using both types of catalyst deposition, the weight ratio of Fe to C-fiber textile was also varied. Ferric particles were reduced to iron after deposition, by using H2/N2 gas, and carbon nanofibers (CNFs) were grown by flowing ethylene gas. Properties of carbon nanofibers created like this were analyzed through Scanning Electron Microscopy (SEM), Energy Dispersive Spectroscopy (EDS), N2-sorption (BET), X-ray Diffraction (XRD), X-ray Photoelectron Spectoscopy (XPS), Thermal analysis (TG/DTA), and Raman spectroscopy. In the case of the deposition-precipitation method, the results show that the diameter of carbon nanofibers grew up to 40-60 nm and 30-55 nm, at which the weight ratios of Fe catalyst to C-fiber textiles were 1:30 and 1:70, respectively. When Fe particles were deposited by the dip-coating method, the diameter of carbon nanofibers grew up to 40-60 nm and 25-30 nm, for the ratios of Fe catalyst to C-fiber textiles of 1:10 and 1:30, respectively. PMID:26716329

  4. Photoemission studies of fluorine functionalized porous graphitic carbon

    SciTech Connect

    Ganegoda, Hasitha; Olive, Daniel; Cheng, Lidens; Segre, Carlo U.; Terry, Jeff; Jensen, David S.; Linford, Matthew R.

    2012-03-01

    Porous graphitic carbon (PGC) has unique properties desirable for liquid chromatography applications when used as a stationary phase. The polar retention effect on graphite (PREG) allows efficient separation of polar and non-polar solutes. Perfluorinated hydrocarbons however lack polarizabilty and display strong lipo- and hydrophobicity, hence common lipophilic and hydrophilic analytes have low partition coefficiency in fluorinated stationary phases. Attractive interaction between fluorinated stationary phase and fluorinated analytes results in strong retention compared to non-fluorinated analytes. In order to change the selectivities of PGC, it is necessary to develop a bonded PGC stationary phase. In this study, we have synthesized perfluorinated, PGC using hepatadecafluoro-1-iodooctane, under different temperature conditions. Surface functionalization of the raw material was studied using photoelectron spectroscopy (PES). Results indicate the existence of fluorine containing functional groups, -CF, -CF{sub 2} along with an intercalated electron donor species. Multiple oxygen functional groups were also observed, likely due to the presence of oxygen in the starting material. These oxygen species may be responsible for significant modifications to planer and tetrahedral carbon ratios.

  5. Photoemission studies of fluorine functionalized porous graphitic carbon

    NASA Astrophysics Data System (ADS)

    Ganegoda, Hasitha; Jensen, David S.; Olive, Daniel; Cheng, Lidens; Segre, Carlo U.; Linford, Matthew R.; Terry, Jeff

    2012-03-01

    Porous graphitic carbon (PGC) has unique properties desirable for liquid chromatography applications when used as a stationary phase. The polar retention effect on graphite (PREG) allows efficient separation of polar and non-polar solutes. Perfluorinated hydrocarbons however lack polarizabilty and display strong lipo- and hydrophobicity, hence common lipophilic and hydrophilic analytes have low partition coefficiency in fluorinated stationary phases. Attractive interaction between fluorinated stationary phase and fluorinated analytes results in strong retention compared to non-fluorinated analytes. In order to change the selectivities of PGC, it is necessary to develop a bonded PGC stationary phase. In this study, we have synthesized perfluorinated, PGC using hepatadecafluoro-1-iodooctane, under different temperature conditions. Surface functionalization of the raw material was studied using photoelectron spectroscopy (PES). Results indicate the existence of fluorine containing functional groups, -CF, -CF2 along with an intercalated electron donor species. Multiple oxygen functional groups were also observed, likely due to the presence of oxygen in the starting material. These oxygen species may be responsible for significant modifications to planer and tetrahedral carbon ratios.

  6. In situ fabrication of Ni(OH){sub 2} nanofibers on polypyrrole-based carbon nanotubes for high-capacitance supercapacitors

    SciTech Connect

    Fan, Jianzhang; Mi, Hongyu; Xu, Youlong; Gao, Bo

    2013-03-15

    Highlights: ► Facile surface decoration approach to highly porous Ni(OH){sub 2}/CNT composites. ► Polypyrrole-based CNTs form three-dimensional electron-transport channels. ► A high capacitance of 1118 F g{sup −1} at 50 mA cm{sup −2} is delivered. ► Ni(OH){sub 2}/CNT composites exhibit high discharge capability. - Abstract: Large-scale nickel hydroxide–carbon [Ni(OH){sub 2}/CNT] networks with three-dimensional electron-transport channels are synthesized via a facile and general surface-decoration approach, using polypyrrole-derived CNTs as the support. Flexible Ni(OH){sub 2} nanofibers with a diameter of 5–10 nm and a length of 50–120 nm are intertwined and wrapped homogenously on carbon networks, leading to the formation of more complex networks. When used as supercapacitor electrodes, this designed architecture with large surface area, abundant pores and good electrical conductivity is very important in technology. It can promote the bulk accessibility of electrolyte OH{sup −} and diffusion rate within the redox phase. Consequently, an unusual specific capacitance of 1745 F g{sup −1} can be obtained for Ni(OH){sub 2}/CNT composite at 30 mA cm{sup −2}. Even at a high rate (50 mA cm{sup −2}), the composite can also deliver a specific capacitance as high as 1118 F g{sup −1}, exhibiting the potential application for supercapacitors.

  7. Synthesis, Optimization, and Performance Demonstration of Electrospun Carbon Nanofiber-Carbon Nanotube Composite Sorbents for Point-of-Use Water Treatment.

    PubMed

    Peter, Katherine T; Vargo, John D; Rupasinghe, Thilini P; De Jesus, Aribet; Tivanski, Alexei V; Sander, Edward A; Myung, Nosang V; Cwiertny, David M

    2016-05-11

    We developed an electrospun carbon nanofiber-carbon nanotube (CNF-CNT) composite with optimal sorption capacity and material strength for point-of-use (POU) water treatment. Synthesis variables including integration of multiwalled carbon nanotubes (CNTs) and macroporosity (via sublimation of phthalic acid), relative humidity (20 and 40%), and stabilization temperature (250 and 280 °C) were used to control nanofiber diameter and surface area (from electron microscopy and BET isotherms, respectively), surface composition (from XPS), and strength (from AFM nanoindentation and tensile strength tests). Composites were then evaluated using kinetic, isotherm, and pH-edge sorption experiments with sulfamethoxazole (log Kow = 0.89) and atrazine (log Kow = 2.61), representative micropollutants chosen for their different polarities. Although CNFs alone were poor sorbents, integration of CNTs and macroporosity achieved uptake comparable to granular activated carbon. Through reactivity comparisons with CNT dispersions, we propose that increasing macroporosity exposes the embedded CNTs, thereby enabling their role as the primary sorbent in nanofiber composites. Because the highest capacity sorbents lacked sufficient strength, our optimal formulation (polyacrylonitrile 8 wt %, CNT 2 wt %, phthalic acid 2.4 wt %; 40% relative humidity; 280 °C stabilization) represents a compromise between strength and performance. This optimized sorbent was tested with a mixture of ten organic micropollutants at environmentally relevant concentrations in a gravity-fed, flow-through filtration system, where removal trends suggest that both hydrophobic and specific binding interactions contribute to micropollutant uptake. Collectively, this work highlights the promise of CNF-CNT filters (e.g., mechanical strength, ability to harness CNT sorption capacity), while also prioritizing areas for future research and development (e.g., improved removal of highly polar micropollutants, sensitivity to

  8. 3D hybrid-porous carbon derived from carbonization of metal organic frameworks for high performance supercapacitors

    NASA Astrophysics Data System (ADS)

    Bao, Weizhai; Mondal, Anjon Kumar; Xu, Jing; Wang, Chengyin; Su, Dawei; Wang, Guoxiu

    2016-09-01

    We report a rational design and synthesis of 3D hybrid-porous carbon with a hierarchical pore architecture for high performance supercapacitors. It contains micropores (<2 nm diameter) and mesopores (2-4 nm), derived from carbonization of unique porous metal organic frameworks (MOFs). Owning to the synergistic effect of micropores and mesopores, the hybrid-porous carbon has exceptionally high ion-accessible surface area and low ion diffusion resistance, which is desired for supercapacitor applications. When applied as electrode materials in supercapacitors, 3D hybrid-porous carbon demonstrates a specific capacitance of 332 F g-1 at a constant charge/discharge current of 500 mA g-1. The supercapacitors can endure more than 10,000 cycles without degradation of capacitance.

  9. Depressing the hydrogenation and decomposition reaction in H2O2 synthesis by supporting AuPD on oxygen functionalized carbon nanofibers

    DOE PAGESBeta

    Villa, Alberto; Freakley, Simon J.; Schiavoni, Marco; Edwards, Jennifer K.; Hammond, Ceri; Wang, Wu; Wang, Di; Prati, Laura; Dimitratos, Nikolaos; Hutchings, Graham J.; et al

    2015-12-03

    In this work, we show that the introduction of acidic oxygen functionalities to the surface of carbon nanofibers serves to depress the hydrogenation and the decomposition of hydrogen peroxide during the direct synthesis of H2O2. Furthermore, the presence of acidic groups enhances the H2O2 productivity in the case of supported AuPd nanoparticles.

  10. Depressing the hydrogenation and decomposition reaction in H2O2 synthesis by supporting gold-palladium nanoparticles on oxygen functionalized carbon nanofibers

    DOE PAGESBeta

    Villa, Alberto; Freakley, Simon J; Schiavoni, Marco; Edwards, Jennifer K; Hammond, Ceri; Wang, Wu; Wang, Di; Prati, Laura; Dimitratos, Nikolaos; Hutchings, Graham J

    2016-01-01

    In this work, we show that the introduction of acidic oxygen functionalities to the surface of carbon nanofibers serves to depress the hydrogenation and the decomposition of hydrogen peroxide during the direct synthesis of H2O2. Moreover, the presence of acidic groups enhances the H2O2 productivity in the case of supported AuPd nanoparticles.

  11. Electrospun silicon/carbon/titanium oxide composite nanofibers for lithium ion batteries

    NASA Astrophysics Data System (ADS)

    Wu, Qingliu; Tran, Toan; Lu, Wenquan; Wu, Ji

    2014-07-01

    Si/C/TiO2 composite nanofibers have been prepared via a facile electrospinning method combined with a sol-gel chemistry, whose electrochemical performance as anode materials in lithium-ion battery was evaluated. As-prepared nanofibers (NFs) were characterized using scanning electron microscopy, energy dispersive spectroscopy, powder X-ray diffraction and thermogravimetric analyzer to identify their morphology, phase, crystallinity and compositions. Rutile phase TiO2 nanofibers demonstrated a relatively low gravimetric specific capacity of ˜83 mAh g-1 when discharged at 0.1C. In contrast, composite nanofibers possess a much higher gravimetric specific capacity. When the Si to C mass ratio is of 0.217, a specific capacity as high as 720 mAh g-1 can be attained, 94% of which can be maintained after 55 cycles. The enhanced cycling stability of micron silicon materials is attributed to the space confinement provided by the structurally stable TiO2. These findings can provide a beneficial guidance for future lithium ion battery electrode development.

  12. Preparation of polyacrylnitrile (PAN)/ Manganese oxide based activated carbon nanofibers (ACNFs) for adsorption of Cadmium (II) from aqueous solution

    NASA Astrophysics Data System (ADS)

    Abdullah, N.; Yusof, N.; Jaafar, J.; Ismail, AF; Che Othman, F. E.; Hasbullah, H.; Salleh, W. N. W.; Misdan, N.

    2016-06-01

    In this work, activated carbon nanofibers (ACNFs) from precursor polyacrylnitrile (PAN) and manganese oxide (MnO2) were prepared via electrospinning process. The electrospun PAN/MnO2-based ACNFs were characterised in term of its morphological structure and specific surface area using SEM and BET analysis respectively. The comparative adsorption study of cadmium (II) ions from aqueous solution between the neat ACNFs, composite ACNFs and commercial granular activated carbon was also conducted. SEM analysis illustrated that composite ACNFs have more compact fibers with presence of MnO2 beads with smaller fiber diameter of 437.2 nm as compared to the neat ACNFs which is 575.5 nm. BET analysis elucidated specific surface area of ACNFs/MnO2 to be 67 m2/g. Under adsorption study, it was found out that Cd (II) removal by ACNFs/MnO2 was the highest (97%) followed by neat ACNFs (96%) and GAC (74%).

  13. Improving interfacial adhesion with epoxy matrix using hybridized carbon nanofibers containing calcium phosphate nanoparticles for bone repairing.

    PubMed

    Gao, Xukang; Lan, Jinle; Jia, Xiaolong; Cai, Qing; Yang, Xiaoping

    2016-04-01

    Hybridized carbon nanofibers containing calcium phosphate nanoparticles (CNF/CaP) were investigated as osteocompatible nanofillers for epoxy resin. The CNF/CaP was produced by electrospinning mixture solution of polyacrylonitrile and CaP precursor sol-gel, followed by preoxidation and carbonization. The continuous and long CNF/CaP was ultrasonically chopped, mixed into epoxy resin and thermo-cured. Compared to pure CNFs with similar ultrasonication treatment, the shortened CNF/CaP reinforced composites demonstrated significant enhancement in flexural properties of epoxy composites, benefiting from the improved interfacial adhesion between CNF/CaP and resin matrix. The resulting composites also displayed good biocompatibility and sustained calcium ion release, which categorized them as promising materials for bone repairing. PMID:26838838

  14. Antimony nanoparticles anchored on interconnected carbon nanofibers networks as advanced anode material for sodium-ion batteries

    NASA Astrophysics Data System (ADS)

    Hou, Hongshuai; Jing, Mingjun; Yang, Yingchang; Zhang, Yan; Song, Weixin; Yang, Xuming; Chen, Jun; Chen, Qiyuan; Ji, Xiaobo

    2015-06-01

    Interconnected carbon nanofibers networks (ICNNs) prepared through the carbonization of polypyrrole (PPy) precursor are utilized as conductive pathways and buffer to improve the Na storage performance of antimony (Sb) as anode for sodium-ion batteries (SIBs). The as-obtained Sb/ICNNs composite exhibits excellent cycle stability. The reversible capacity can remain 542.5 mAh g-1 with a high capacity retention of 96.7% after 100 cycles at a current density of 100 mA g-1. And the superior rate performance is also observed, the reversible capacity can still reach 325 mAh g-1 at a high current density of 3200 mA g-1. These great electrochemical performances observed above suggest that this type of composite can be a nice option for advanced SIBs anode materials and may be extended to other active materials/ICNNs composite electrode.

  15. Highly flexible NiCo2O4/CNTs doped carbon nanofibers for CO2 adsorption and supercapacitor electrodes.

    PubMed

    Iqbal, Nousheen; Wang, Xianfeng; Ahmed Babar, Aijaz; Yu, Jianyong; Ding, Bin

    2016-08-15

    Controllable synthesis of carbon nanofibers (CNFs) with hierarchical porosity and high flexibility are extremely desirable for CO2 adsorption and energy storage applications. Herein, we report a nickel cobaltite/carbon nanotubes doped CNFs (NiCo2O4/CNTs CNFs) mesoporous membrane that shows well-developed flexibility, tailored pore structure, hydrophobic character, and high stability. Ascribed to these unique features, NiCo2O4/CNTs CNFs membrane shows high CO2 capture of 1.54mmol/g at 25°C and 1.0bar, and electrochemical measurements for supercapacitors exhibit good performance with specific capacitances of 220F/g (in 1M KOH) at a current density of 1A/g. The successful synthesis of such hybrid membrane provides new insight into development of various multifunctional applications. PMID:27209394

  16. A carbon nanofiber based biosensor for simultaneous detection of dopamine and serotonin in the presence of ascorbic acid

    PubMed Central

    Rand, Emily; Periyakaruppan, Adaikkappan; Tanaka, Zuki; Zhang, David; Marsh, Michael P.; Andrews, Russell J.; Lee, Kendall H.; Chen, Bin; Meyyappan, M.; Koehne, Jessica E.

    2013-01-01

    A biosensor based on an array of vertically aligned carbon nanofibers (CNFs) grown by plasma enhanced chemical vapor deposition is found to be effective for the simultaneous detection of dopamine (DA) and serotonin (5-HT) in the presence of excess ascorbic acid (AA). The CNF electrode outperforms the conventional glassy carbon electrode (GCE) for both selectivity and sensitivity. Using differential pulse voltammetry (DPV), three distinct peaks are seen for the CNF electrode at 0.13 V, 0.45 V, and 0.70 V for the ternary mixture of AA, DA, and 5-HT. In contrast, the analytes are indistinguishable in a mixture using a GCE. For the CNF electrode, the detection limits are 50 nM for DA and 250 nM for 5-HT. PMID:23228495

  17. A carbon nanofiber based biosensor for simultaneous detection of dopamine and serotonin in the presence of ascorbic acid.

    PubMed

    Rand, Emily; Periyakaruppan, Adaikkappan; Tanaka, Zuki; Zhang, David A; Marsh, Michael P; Andrews, Russell J; Lee, Kendall H; Chen, Bin; Meyyappan, M; Koehne, Jessica E

    2013-04-15

    A biosensor based on an array of vertically aligned carbon nanofibers (CNFs) grown by plasma enhanced chemical vapor deposition is found to be effective for the simultaneous detection of dopamine (DA) and serotonin (5-HT) in the presence of excess ascorbic acid (AA). The CNF electrode outperforms the conventional glassy carbon electrode (GCE) for both selectivity and sensitivity. Using differential pulse voltammetry (DPV), three distinct peaks are seen for the CNF electrode at 0.13 V, 0.45 V, and 0.70 V for the ternary mixture of AA, DA, and 5-HT. In contrast, the analytes are indistinguishable in a mixture using a GCE. For the CNF electrode, the detection limits are 50 nM for DA and 250 nM for 5-HT. PMID:23228495

  18. Glutathione modified screen-printed carbon nanofiber electrode for the voltammetric determination of metal ions in natural samples.

    PubMed

    Pérez-Ràfols, Clara; Serrano, Núria; Díaz-Cruz, José Manuel; Ariño, Cristina; Esteban, Miquel

    2016-08-01

    This work reports the development of a glutathione modified electrode via electrografting on a screen-printed carbon nanofiber substrate (GSH-SPCNFE). GSH-SPCNFE was compared to a classical screen-printed carbon electrode modified with glutathione (GSH-SPCE) for the simultaneous voltammetric determination of Cd(II) and Pb(II). Their electrochemical characterization and analytical performance suggest that SPCNFE could be a much better support for GSH immobilization. The applicability of GSH-SPCNFE for the determination of low concentration levels of Pb(II) and Cd(II) ions in environmental samples was successfully tested in a certified wastewater reference material by means of stripping voltammetry with a very high reproducibility and good trueness. PMID:27216650

  19. Single-Walled Carbon Nanotubes, Carbon Nanofibers and Laser-Induced Incandescence

    NASA Technical Reports Server (NTRS)

    Schubert, Kathy (Technical Monitor); VanderWal, Randy L.; Ticich, Thomas M.; Berger, Gordon M.; Patel, Premal D.

    2004-01-01

    Laser induced incandescence applied to a heterogeneous, multi-element reacting flows is characterized by a) temporally resolved emission spectra, time-resolved emission at selected detection wavelengths and fluence dependence. Laser fluences above 0.6 Joules per square centimeter at 1064 nm initiate laser-induced vaporization, yielding a lower incandescence intensity, as found through fluence dependence measurements. Spectrally derived temperatures show that values of excitation laser fluence beyond this value lead to a super-heated plasma, well above the vaporization of temperature of carbon. The temporal evolution of the emission signal at these fluences is consistent with plasma dissipation processes, not incandescence from solid-like structures.

  20. Effects of increasing carbon nanofiber density in polyurethane composites for inhibiting bladder cancer cell functions.

    PubMed

    Tsang, Melissa; Chun, Young Wook; Im, Yeon Min; Khang, Dongwoo; Webster, Thomas J

    2011-07-01

    Polyurethane (PU) is a versatile elastomer that is commonly used in biomedical applications. In turn, materials derived from nanotechnology, specifically carbon nanofibers (CNFs), have received increasing attention for their potential use in biomedical applications. Recent studies have shown that the dispersion of CNFs in PU significantly enhances composite nanoscale surface roughness, tensile properties, and thermal stability. Although there have been studies concerning normal primary cell functions on such nanocomposites, there have been few studies detailing cancer cell responses. Since many patients who require bladder transplants have suffered from bladder cancer, the ideal bladder prosthetic material should not only promote normal primary human urothelial cell (HUC) function, but also inhibit the return of bladder cancerous cell activity. This study examined the correlation between transitional (UMUC) and squamous (or SCaBER) urothelial carcinoma cells and HUC on PU:CNF nanocomposites of varying PU and CNF weight ratios (from pure PU to 4:1 [PU:CNF volume ratios], 2:1, 1:1, 1:2, and 1:4 composites to pure CNF). Composites were characterized for mechanical properties, wettability, surface roughness, and chemical composition by atomic force microscopy, scanning electron microscopy, X-ray photoelectron spectroscopy, Fourier-transform infrared spectroscopy, and goniometry. The adhesion and proliferation of UMUC and SCaBER cancer cells were assessed by MTS assays. Cellular responses were further quantified by measuring the amounts of nuclear mitotic protein 22 (NMP-22), vascular endothelial growth factor (VEGF), and tumor necrosis factor alpha. Results demonstrated that both UMUC and SCaBER cell proliferation rates decreased over time on substrates with increased CNF in PU. In addition, with the exception of VEGF from UMUC (which was the same across all materials), composites containing the most CNF activated cancer cells (UMUC and SCaBER) the least, as shown by

  1. Disposal of Liquid Combustible Wastes using Flameless Burners with Porous Carbon Matrix

    NASA Astrophysics Data System (ADS)

    Dolgov, Sergei; Savchenko, Evgenii; Khaustov, Sergei; Tabakaev, Roman; Zavorin, Alexander

    2016-02-01

    Two modifications of flameless burners with a carbon porous media in the combustion area were investigated. Kerosene TS-1 and mixtures of highly flammable liquids wastes (HIL) were used as fuel. Experimental data are presented in a graphical form as plot of the burner thermal capacity. Results show capacity for of the developed devices and prove the prospects of disposal of liquid combustible wastes using flameless burners with porous carbon matrix.

  2. Carbon and Binder-Free Air Electrodes Composed of Co3O4 Nanofibers for Li-Air Batteries with Enhanced Cyclic Performance

    NASA Astrophysics Data System (ADS)

    Lee, Chan Kyu; Park, Yong Joon

    2015-08-01

    In this study, to fabricate a carbon free (C-free) air electrode, Co3O4 nanofibers were grown directly on a Ni mesh to obtain Co3O4 with a high surface area and good contact with the current collector (the Ni mesh). In Li-air cells, any C present in the air electrode promotes unwanted side reactions. Therefore, the air electrode composed of only Co3O4 nanofibers (i.e., C-free) was expected to suppress these side reactions, such as the decomposition of the electrolyte and formation of Li2CO3, which would in turn enhance the cyclic performance of the cell. As predicted, the Co3O4-nanofiber electrode successfully reduced the accumulation of reaction products during cycling, which was achieved through the suppression of unwanted side reactions. In addition, the cyclic performance of the Li-air cell was superior to that of a standard electrode composed of carbonaceous material.

  3. Studies on the reactive melt infiltration of silicon and silicon-molybdenum alloys in porous carbon

    NASA Technical Reports Server (NTRS)

    Singh, M.; Behrendt, D. R.

    1992-01-01

    Investigations on the reactive melt infiltration of silicon and silicon-1.7 and 3.2 at percent molybdenum alloys into porous carbon preforms have been carried out by process modeling, differential thermal analysis (DTA) and melt infiltration experiments. These results indicate that the initial pore volume fraction of the porous carbon preform is a critical parameter in determining the final composition of the raction-formed silicon carbide and other residual phases. The pore size of the carbon preform is very detrimental to the exotherm temperatures due to liquid silicon-carbon reactions encountered during the reactive melt infiltration process. A possible mechanism for the liquid silicon-porous (glassy) carbon reaction has been proposed. The composition and microstructure of the reaction-formed silicon carbide has been discussed in terms of carbon preform microstructures, infiltration materials, and temperatures.

  4. Studies on the reactive melt infiltration of silicon and silicon-molybdenum alloys in porous carbon

    SciTech Connect

    Singh, M.; Behrendt, D.R.

    1992-09-01

    Investigations on the reactive melt infiltration of silicon and silicon-1.7 and 3.2 at percent molybdenum alloys into porous carbon preforms have been carried out by process modeling, differential thermal analysis (DTA) and melt infiltration experiments. These results indicate that the initial pore volume fraction of the porous carbon preform is a critical parameter in determining the final composition of the reaction-formed silicon carbide and other residual phases. The pore size of the carbon preform is very detrimental to the exotherm temperatures due to liquid silicon-carbon reactions encountered during the reactive melt infiltration process. A possible mechanism for the liquid silicon-porous (glassy) carbon reaction has been proposed. The composition and microstructure of the reaction-formed silicon carbide has been discussed in terms of carbon preform microstructures, infiltration materials, and temperatures.

  5. Imaging, Spectroscopic, Mechanical and Biocompatibility Studies of Electrospun Tecoflex(®) EG 80A Nanofibers and Composites Thereof Containing Multiwalled Carbon Nanotubes.

    PubMed

    Macossay, Javier; Sheikh, Faheem A; Cantu, Travis; Eubanks, Thomas M; Salinas, M Esther; Farhangi, Chakavak S; Ahmad, Hassan; Hassan, M Shamshi; Khil, Myung-Seob; Maffi, Shivani K; Kim, Hern; Bowlin, Gary L

    2014-12-01

    The present study discusses the design, development and characterization of electrospun Tecoflex(®) EG 80A class of polyurethane nanofibers and the incorporation of multiwalled carbon nanotubes (MWCNTs) to these materials. Scanning electron microscopy results confirmed the presence of polymer nanofibers, which showed a decrease in fiber diameter at 0.5% wt. and 1% wt. MWCNTs loadings, while transmission electron microscopy showed evidence of the MWCNTs embedded within the polymer matrix. The fourier transform infrared spectroscopy and Raman spectroscopy were used to elucidate the polymer-MWCNTs intermolecular interactions, indicating that the C-N and N-H bonds in polyurethanes are responsible for the interactions with MWCNTs. Furthermore, tensile testing indicated an increase in the Young's modulus of the nanofibers as the MWCNTs concentration was increased. Finally, NIH 3T3 fibroblasts were seeded on the obtained nanofibers, demonstrating cell biocompatibility and proliferation. Therefore, the results indicate the successful formation of polyurethane nanofibers with enhanced mechanical properties, and demonstrate their biocompatibility, suggesting their potential application in biomedical areas. PMID:25435600

  6. Imaging, Spectroscopic, Mechanical and Biocompatibility Studies of Electrospun Tecoflex® EG 80A Nanofibers and Composites Thereof Containing Multiwalled Carbon Nanotubes

    PubMed Central

    Macossay, Javier; Sheikh, Faheem A.; Cantu, Travis; Eubanks, Thomas M.; Salinas, M. Esther; Farhangi, Chakavak S.; Ahmad, Hassan; Hassan, M. Shamshi; Khil, Myung-seob; Maffi, Shivani K.; Kim, Hern; Bowlin, Gary l.

    2014-01-01

    The present study discusses the design, development and characterization of electrospun Tecoflex® EG 80A class of polyurethane nanofibers and the incorporation of multiwalled carbon nanotubes (MWCNTs) to these materials. Scanning electron microscopy results confirmed the presence of polymer nanofibers, which showed a decrease in fiber diameter at 0.5% wt. and 1% wt. MWCNTs loadings, while transmission electron microscopy showed evidence of the MWCNTs embedded within the polymer matrix. The fourier transform infrared spectroscopy and Raman spectroscopy were used to elucidate the polymer-MWCNTs intermolecular interactions, indicating that the C-N and N-H bonds in polyurethanes are responsible for the interactions with MWCNTs. Furthermore, tensile testing indicated an increase in the Young’s modulus of the nanofibers as the MWCNTs concentration was increased. Finally, NIH 3T3 fibroblasts were seeded on the obtained nanofibers, demonstrating cell biocompatibility and proliferation. Therefore, the results indicate the successful formation of polyurethane nanofibers with enhanced mechanical properties, and demonstrate their biocompatibility, suggesting their potential application in biomedical areas. PMID:25435600

  7. Carbon/SnO2/carbon core/shell/shell hybrid nanofibers: tailored nanostructure for the anode of lithium ion batteries with high reversibility and rate capacity

    NASA Astrophysics Data System (ADS)

    Kong, Junhua; Liu, Zhaolin; Yang, Zhengchun; Tan, Hui Ru; Xiong, Shanxin; Wong, Siew Yee; Li, Xu; Lu, Xuehong

    2012-01-01

    A carbon/SnO2/carbon core/shell/shell hybrid nanofibrous mat was successfully prepared via single-spinneret electrospinning followed by carbonization and hydrothermal treatment. The morphology and structure of carbon/SnO2/carbon hybrid nanofibers were characterized by field-emission scanning electron microscopy, transmission electron microscopy, thermogravimetric analysis, wide-angle X-ray diffraction and X-ray photoelectron spectroscopy, and their electrochemical properties were studied as an anode in lithium ion batteries (LIBs). It is shown that the designed hybrid nanofibrous mat exhibits excellent electrochemical properties, including high reversible capacity with high columbic efficiency and impressive rate capacity. The greatly enhanced electrochemical performance is mainly due to the morphological stability and reduced diffusion resistance, which are induced by both the carbon core and deposited carbon skin. Furthermore, the embedded and de-aggregated SnO2 nanoparticles in the carbon phase, which are less than 10 nm in size, provide large numbers of reaction sites for lithium ions and ensure complete alloying with them.A carbon/SnO2/carbon core/shell/shell hybrid nanofibrous mat was successfully prepared via single-spinneret electrospinning followed by carbonization and hydrothermal treatment. The morphology and structure of carbon/SnO2/carbon hybrid nanofibers were characterized by field-emission scanning electron microscopy, transmission electron microscopy, thermogravimetric analysis, wide-angle X-ray diffraction and X-ray photoelectron spectroscopy, and their electrochemical properties were studied as an anode in lithium ion batteries (LIBs). It is shown that the designed hybrid nanofibrous mat exhibits excellent electrochemical properties, including high reversible capacity with high columbic efficiency and impressive rate capacity. The greatly enhanced electrochemical performance is mainly due to the morphological stability and reduced diffusion

  8. A novel strategy to synthesize hierarchical, porous carbohydrate-derived carbon with tunable properties

    NASA Astrophysics Data System (ADS)

    Wang, Shiping; Liu, Ruihan; Han, Chuanlong; Wang, Jing; Li, Mingming; Yao, Jia; Li, Haoran; Wang, Yong

    2014-10-01

    Hydrothermal carbonization (HTC) of carbohydrate is an interesting candidate for the preparation of carbon materials, as it provides an easy, inexpensive and environmental friendly route. However, it is difficult to prepare porous carbon materials by a straight HTC process. Herein, the solubilising technology of micelles was introduced to direct the HTC of fructose by using an amphiphilic block copolymer, poly-(4-vinylpyridine)-block-poly-(ethylene glycol) (P4VP-PEG), as a structure-directing agent. By this strategy, hierarchical porous carbon materials with tunable properties were prepared. It was found that P4VP-PEG micelles could solubilize fructose and confine the formation of primary carbon domains during a sol-gel process. And the micelle size could be adjusted easily by changing the preparation conditions. Accordingly, the particle size of the obtained carbon materials was effectively tuned from 20 to 100 nm by the direction of the primary micelle size. After calcination, the hierarchical porous carbon materials were evidenced as effective electrode materials for supercapacitor with a capacitance of ~197 F at 1 A g-1, which was almost four times higher than the carbon materials prepared by a straight HTC process.Hydrothermal carbonization (HTC) of carbohydrate is an interesting candidate for the preparation of carbon materials, as it provides an easy, inexpensive and environmental friendly route. However, it is difficult to prepare porous carbon materials by a straight HTC process. Herein, the solubilising technology of micelles was introduced to direct the HTC of fructose by using an amphiphilic block copolymer, poly-(4-vinylpyridine)-block-poly-(ethylene glycol) (P4VP-PEG), as a structure-directing agent. By this strategy, hierarchical porous carbon materials with tunable properties were prepared. It was found that P4VP-PEG micelles could solubilize fructose and confine the formation of primary carbon domains during a sol-gel process. And the micelle size

  9. Effects of feed gas composition and catalyst thickness on carbon nanotube and nanofiber synthesis by plasma enhanced chemical vapor deposition.

    PubMed

    Garg, R K; Kim, S S; Hash, D B; Gore, J P; Fisher, T S

    2008-06-01

    Many engineering applications require carbon nanotubes with specific characteristics such as wall structure, chirality and alignment. However, precise control of nanotube properties grown to application specifications remains a significant challenge. Plasma-enhanced chemical vapor deposition (PECVD) offers a variety of advantages in the synthesis of carbon nanotubes in that several important synthesis parameters can be controlled independently. This paper reports an experimental study of the effects of reacting gas composition (percentage methane in hydrogen) and catalyst film thickness on carbon nanotube (CNT) growth and a computational study of gas-phase composition for the inlet conditions of experimentally observed carbon nanotube growth using different chemical reaction mechanisms. The simulations seek to explain the observed effects of reacting gas composition and to identify the precursors for CNT formation. The experimental results indicate that gas-phase composition significantly affects the synthesized material, which is shown to be randomly aligned nanotube and nanofiber mats for relatively methane-rich inlet gas mixtures and non-tubular carbon for methane-lean incoming mixtures. The simulation results suggest that inlet methane-hydrogen mixture coverts to an acetylene-methane-hydrogen mixture with minor amounts of ethylene, hydrogen atom, and methyl radical. Acetylene appears to be the indicator species for solid carbon formation. The simulations also show that inlet methane-hydrogen mixture does not produce enough gas-phase precursors needed to form quality CNTs below 5% CH4 concentrations in the inlet stream. PMID:18681048

  10. Mechanical and electromagnetic interference shielding Properties of poly(vinyl alcohol)/graphene and poly(vinyl alcohol)/multi-walled carbon nanotube composite nanofiber mats and the effect of Cu top-layer coating.

    PubMed

    Fujimori, Kazushige; Gopiraman, Mayakrishnan; Kim, Han-Ki; Kim, Byoung-Suhk; Kim, Ick-Soo

    2013-03-01

    We report the mechanical property and electromagnetic interference shielding effectiveness (EMI SE) of poly(vinyl alcohol) (PVA)/graphene and PVA/multi-walled carbon nanotube (MWCNT) composite nanofibers prepared by electrospinning. The metal (Cu) was deposited on the resultant PVA composite nanofibers using metal deposition technique in order to improve the mechanical properties and EMI shielding properties. The resulting PVA composite nanofibers and Cu-deposited corresponding nanofibers were characterized by field emission scanning electron microscopy (FE-SEM), transmission electron microscopy (TEM) and wide angle X-ray diffraction (WAXD). Tensile tests were performed on the PVA/graphene and PVA/MWCNT composite nanofibers. The tensile strength of the PVA/graphene and PVA/MWCNT composite nanofibers was found to be 19.2 +/- 0.3 MPa at graphene content - 6.0 wt% and 12.2 +/- 0.2 MPa at MWCNT content - 3.0 wt%, respectively. The EMI SE of the Cu-deposited PVA/graphene composite nanofibers was significantly improved compared to pure PVA/graphene composite nanofibers, and also depended on the thickness of Cu metal layer deposited on the PVA composite nanofibers. PMID:23755586

  11. Viscoelastic characterization of vapor-grown carbon nanofiber/vinyl ester nanocomposites using a response surface methodology

    NASA Astrophysics Data System (ADS)

    Drake, Daniel Adam

    The effects of vapor-grown carbon nanofiber (VGCNF) weight fraction, applied stress, and temperature on the viscoelastic responses (creep strain, creep rate, and creep compliance) of VGCNF/vinyl ester (VE) nanocomposites were studied using a central composite design (CCD). The nanocomposite test articles were fabricated by high shear mixing, casting, curing, and post-curing in an open face mold under a nitrogen environment. Short-term creep/creep recovery experiments were conducted at prescribed combinations of temperatures (23.8 - 69.2 C), applied stresses (30.2 - 49.8 MPa), and VGCNF weight fractions (0.00 - 1.00 parts of VGCNF per hundred parts of resin, phr) determined from the CCD. The response surface models (RSMs) for predicting these viscoelastic responses were developed using the least squares method and an analysis of variance procedure. The response surface estimates indicate that increasing the VGCNF weight fraction marginally increases the creep resistance of the VGCNF/VE nanocomposite at low temperatures (i.e., 23.8 - 46.5 C). However, increasing the VGCNF weight fraction for temperatures greater than 50 C decreased the creep resistance of these nanocomposites. The latter response may be due to a decrease in the nanofiber-to-matrix adhesion as the temperature is increased. The RSMs for creep strain, creep rate, and creep compliance revealed the interactions between the VGCNF weight fraction, stress, and temperature on the creep behavior of thermoset polymer.

  12. Vapor-phase polymerization of poly(3, 4-ethylenedioxythiophene) nanofibers on carbon cloth as electrodes for flexible supercapacitors.

    PubMed

    Zhao, Xin; Dong, Mengyang; Zhang, Junxian; Li, Yingzhi; Zhang, Qinghua

    2016-09-23

    In this study, an evaporative vapor-phase polymerization approach was employed to fabricate vertically aligned poly(3, 4-ethylenedioxythiophene) (PEDOT) nanofibers on the surface of carbon cloth (CC). Optimized reaction conditions can obtain well distributed and uniform layers of high-aspect-ratio PEDOT nanofibers on CC. The hierarchical PEDOT/CC structure as a freestanding electrode exhibits good electrochemical properties. As a flexible symmetric supercapacitor, the PEDOT/CC hybrid electrode displays a specific areal capacitance of 201.4 mF cm(-2) at 1 mA cm(-2), good flexibility with a higher value (204.6 mF cm(-2)) in the bending state, and a good cycling stability of 92.4% after 1000 cycles. Moreover, the device shows a maximum energy density of 4.0 Wh kg(-1) (with a power density of 3.2 kW kg(-1)) and a maximum power density of 4.2 kW kg(-1) (with an energy density of 3.1 Wh kg(-1)). The results demonstrate that PEDOT may be a promising material for storage devices through a simple and efficient vapor-phase polymerization process with precisely controlled reaction conditions. PMID:27533130

  13. Metal-Support Interactions of Platinum Nanoparticles Decorated N-Doped Carbon Nanofibers for the Oxygen Reduction Reaction.

    PubMed

    Melke, Julia; Peter, Benedikt; Habereder, Anja; Ziegler, Juergen; Fasel, Claudia; Nefedov, Alexei; Sezen, Hikmet; Wöll, Christof; Ehrenberg, Helmut; Roth, Christina

    2016-01-13

    N-doped carbon materials are discussed as catalyst supports for the electrochemical oxygen reduction reaction (ORR) in fuel cells. This work deals with the preparation of Pt nanoparticles (NPs) supported on N-doped carbon nanofibers (N-CNF) from a polyaniline nanofiber (PANI NF) precursor, and investigates the ORR activity of the produced materials. Initially, Pt NPs are deposited on PANI NFs. The PANI NF precursors are characterized by near-edge X-ray absorption fine structure (NEXAFS) and transmission electron microscopy (TEM) measurements. It is shown, that in the PANI NF precursor materials electrons from the Pt are being transferred toward the π-conjugated systems of the aromatic ring. This strong interaction of Pt atoms with PANI explains the high dispersion of Pt NPs on the PANI NF. Subsequently, the PANI NF precursors are carbonized at different heat-treatment conditions resulting in structurally different N-CNFs which are characterized by NEXAFS, X-ray photoelectron spectroscopy (XPS) ,and TEM measurements. It is shown that an interaction between N-groups and Pt NPs exists in all investigated N-CNFs. However, the N-CNFs differ in the composition of the N-species and the dispersion of the Pt NPs. A small mean Pt NP size with a narrow size distribution is attributed to the presence of pyrdinic N-groups in the N-CNFs, whereas, for the N-CNFs with mainly graphitic and pyrrolic N-groups, an increase in the average Pt NP size with a broad size distribution is found. The ORR activity in alkaline media investigated by Koutecky-Levich analysis of rotating disk electrode measurements showed a largely enhanced ORR activity in comparison to a conventional Pt/C catalyst. PMID:26673813

  14. Nondestructive evaluation of ±45° flat-braided carbon-fiber-reinforced polymers with carbon nanofibers using HTS-SQUID gradiometer

    NASA Astrophysics Data System (ADS)

    Hatsukade, Y.; Shinyama, Y.; Yoshida, K.; Takai, Y.; Aly-Hassan, M. S.; Nakai, A.; Hamada, H.; Adachi, S.; Tanabe, K.; Tanaka, S.

    2013-01-01

    Step-by-step tensile tests were applied to flat-braided carbon-fiber-reinforced polymers with and without added dispersions of carbon nanofibers (CNFs) and with and without sample sides cut off to study their mechanical properties and destructive mechanisms by means of in situ observation and stress-strain measurements. An ex situ nondestructive evaluation technique, using a high-temperature superconductor superconducting quantum interference device gradiometer, was also applied to the samples to study their electrical properties; the relationships between the mechanical and electrical properties by visualizing current maps in the samples during ac current injection was also studied. Clear differences were observed in the mechanical and electrical properties and the destructive mechanisms between the samples with and without CNFs and with and without cut off sides. These differences were mainly attributed to the addition of CNFs, which enhanced the mechanical and electrical connections between the carbon fiber bundles.

  15. Multifunctional Ag-decorated porous TiO2 nanofibers in dye-sensitized solar cells: efficient light harvesting, light scattering, and electrolyte contact.

    PubMed

    Hwang, Sun Hye; Song, Hee; Lee, Jungsup; Jang, Jyongsik

    2014-09-26

    Designing the photoanode structure in dye-sensitized solar cells (DSSCs) is vital to realizing enhanced power conversion efficiency (PCE). Herein, novel multifunctional silver-decorated porous titanium dioxide nanofibers (Ag/pTiO2 NFs) made by simple electrospinning, etching, and chemical reduction processes are introduced. The Ag/pTiO2 NFs with a high surface area of 163 m(2)  g(-1) provided sufficient dye adsorption for light harvesting. Moreover, the approximately 200 nm diameter and rough surface of the Ag/pTiO2 NFs offered enough light scattering, and the enlarged interpores among the NFs in the photoanode also permitted electrolyte circulation. Ag nanoparticles (NPs) were well dispersed on the surface of the TiO2 NFs, which prevented aggregation of the Ag NPs after calcination. Furthermore, a localized surface plasmon resonance effect by the Ag NPs served to increase the light absorption at visible wavelengths. The surface area and amount of Ag NPs was optimized. The PCE of pTiO2 NF-based DSSCs was 27 % higher (from 6.2 to 7.9 %) than for pure TiO2 NFs, whereas the PCE of Ag/pTiO2 NF-based DSSCs increased by about 12 % (from 7.9 to 8.8 %). Thus, the PCE of the multifunctional pTiO2 NFs was improved by 42 %, that is, from 6.2 to 8.8 %. PMID:25138442

  16. Two-Dimensional Porous Carbon: Synthesis and Ion-Transport Properties.

    PubMed

    Zheng, Xiaoyu; Luo, Jiayan; Lv, Wei; Wang, Da-Wei; Yang, Quan-Hong

    2015-09-23

    Their chemical stability, high specific surface area, and electric conductivity enable porous carbon materials to be the most commonly used electrode materials for electrochemical capacitors (also known as supercapacitors). To further increase the energy and power density, engineering of the pore structures with a higher electrochemical accessible surface area, faster ion-transport path and a more-robust interface with the electrolyte is widely investigated. Compared with traditional porous carbons, two-dimensional (2D) porous carbon sheets with an interlinked hierarchical porous structure are a good candidate for supercapacitors due to their advantages in high aspect ratio for electrode packing and electron transport, hierarchical pore structures for ion transport, and short ion-transport length. Recent progress on the synthesis of 2D porous carbons is reported here, along with the improved electrochemical behavior due to enhanced ion transport. Challenges for the controlled preparation of 2D porous carbons with desired properties are also discussed; these require precise tuning of the hierarchical structure and a clarification of the formation mechanisms. PMID:26207982

  17. Template-free synthesis of porous graphitic carbon nitride/carbon composite spheres for electrocatalytic oxygen reduction reaction.

    PubMed

    Fu, Xiaorui; Hu, Xiaofei; Yan, Zhenhua; Lei, Kaixiang; Li, Fujun; Cheng, Fangyi; Chen, Jun

    2016-01-28

    Porous graphitic carbon nitride/carbon composite spheres were synthesized using melamine and cyanuric acid, and glucose as the carbon nitride and carbon precursor, respectively. The 3D hierarchical composites efficiently catalyzed the oxygen reduction reaction with an onset potential of 0.90 V and a kinetic current density of 23.92 mA cm(-2). These merit their promising applications in fuel cells and metal-air batteries. PMID:26666314

  18. Preparation of a new adsorbent from activated carbon and carbon nanofiber (AC/CNF) for manufacturing organic-vacbpour respirator cartridge

    PubMed Central

    2013-01-01

    In this study a composite of activated carbon and carbon nanofiber (AC/CNF) was prepared to improve the performance of activated carbon (AC) for adsorption of volatile organic compounds (VOCs) and its utilization for respirator cartridges. Activated carbon was impregnated with a nickel nitrate catalyst precursor and carbon nanofibers (CNF) were deposited directly on the AC surface using catalytic chemical vapor deposition. Deposited CNFs on catalyst particles in AC micropores, were activated by CO2 to recover the surface area and micropores. Surface and textural characterizations of the prepared composites were investigated using Brunauer, Emmett and Teller’s (BET) technique and electron microscopy respectively. Prepared composite adsorbent was tested for benzene, toluene and xylene (BTX) adsorption and then employed in an organic respirator cartridge in granular form. Adsorption studies were conducted by passing air samples through the adsorbents in a glass column at an adjustable flow rate. Finally, any adsorbed species not retained by the adsorbents in the column were trapped in a charcoal sorbent tube and analyzed by gas chromatography. CNFs with a very thin diameter of about 10-20 nm were formed uniformly on the AC/CNF. The breakthrough time for cartridges prepared with CO2 activated AC/CNF was 117 minutes which are significantly longer than for those cartridges prepared with walnut shell- based activated carbon with the same weight of adsorbents. This study showed that a granular form CO2 activated AC/CNF composite could be a very effective alternate adsorbent for respirator cartridges due to its larger adsorption capacities and lower weight. PMID:23369424

  19. Facile preparation of hierarchically porous carbons from metal-organic gels and their application in energy storage

    PubMed Central

    Xia, Wei; Qiu, Bin; Xia, Dingguo; Zou, Ruqiang

    2013-01-01

    Porous carbon materials have numerous applications due to their thermal and chemical stability, high surface area and low densities. However, conventional preparing porous carbon through zeolite or silica templates casting has been criticized by the costly and/or toxic procedure. Creating three-dimensional (3D) carbon products is another challenge. Here, we report a facile way to prepare porous carbons from metal-organic gel (MOG) template, an extended metal-organic framework (MOF) structure. We surprisingly found that the carbon products inherit the highly porous nature of MOF and combine with gel's integrated character, which results in hierarchical porous architectures with ultrahigh surface areas and quite large pore volumes. They exhibit considerable hydrogen uptake and excellent electrochemical performance as cathode material for lithium-sulfur battery. This work provides a general method to fast and clean synthesis of porous carbon materials and opens new avenues for the application of metal-organic gel in energy storage. PMID:23728472

  20. Polymeric Nanofibers in Tissue Engineering

    PubMed Central

    Dahlin, Rebecca L.; Kasper, F. Kurtis

    2011-01-01

    Polymeric nanofibers can be produced using methods such as electrospinning, phase separation, and self-assembly, and the fiber composition, diameter, alignment, degradation, and mechanical properties can be tailored to the intended application. Nanofibers possess unique advantages for tissue engineering. The small diameter closely matches that of extracellular matrix fibers, and the relatively large surface area is beneficial for cell attachment and bioactive factor loading. This review will update the reader on the aspects of nanofiber fabrication and characterization important to tissue engineering, including control of porous structure, cell infiltration, and fiber degradation. Bioactive factor loading will be discussed with specific relevance to tissue engineering. Finally, applications of polymeric nanofibers in the fields of bone, cartilage, ligament and tendon, cardiovascular, and neural tissue engineering will be reviewed. PMID:21699434

  1. The development, fabrication, and material characterization of polypropylene composites reinforced with carbon nanofiber and hydroxyapatite nanorod hybrid fillers

    PubMed Central

    Liao, Cheng Zhu; Wong, Hoi Man; Yeung, Kelvin Wai Kwok; Tjong, Sie Chin

    2014-01-01

    This study focuses on the design, fabrication, microstructural and property characterization, and biocompatibility evaluation of polypropylene (PP) reinforced with carbon nanofiber (CNF) and hydroxyapatite nanorod (HANR) fillers. The purpose is to develop advanced PP/CNF–HANR hybrids with good mechanical behavior, thermal stability, and excellent biocompatibility for use as craniofacial implants in orthopedics. Several material-examination techniques, including X-ray diffraction, Fourier-transform infrared spectroscopy, scanning electron microscopy, thermogravimetric analysis, differential scanning calorimetry, tensile tests, and impact measurement are used to characterize the microstructural, mechanical, and thermal properties of the hybrids. Furthermore, osteoblastic cell cultivation and colorimetric assay are also employed for assessing their viability on the composites. The CNF and HANR filler hybridization yields an improvement in Young’s modulus, impact strength, thermal stability, and biocompatibility of PP. The PP/2% CNF–20% HANR hybrid composite is found to exhibit the highest elastic modulus, tensile strength, thermal stability, and biocompatibility. PMID:24648729

  2. Local Structure Determination of Carbon/Nickel Ferrite Composite Nanofibers Probed by X-ray Absorption Spectroscopy.

    PubMed

    Nilmoung, Sukunya; Kidkhunthod, Pinit; Maensiri, Santi

    2015-11-01

    Carbon/NiFe2O4 composite nanofibers have been successfully prepared by electrospinning method using a various concentration solution of Ni and Fe nitrates dispersed into polyacrylonitride (PAN) solution in N,N' dimethylformamide. The phase and mophology of PAN/NiFe2O4 composite samples were characterized and investigated by X-ray diffraction and scanning electron microscopy. The magnetic properties of the prepared samples were measured at ambient temperature by a vibrating sample magnetometer. It is found that all composite samples exhibit ferromagnetism. This could be local-structurally explained by the existed oxidation states of Ni2+ and Fe3+ in the samples. Moreover, local environments around Ni and Fe ions could be revealed by X-ray absorption spectroscopy (XAS) measurement including X-ray absorption near edge structure (XANES) and Extended X-ray absorption fine structure (EXAFS). PMID:26726677

  3. Enhanced catalytic activity of polyethylenedioxythiophene towards tri-iodide reduction in DSSCs via 1-dimensional alignment using hollow carbon nanofibers

    NASA Astrophysics Data System (ADS)

    Anothumakkool, Bihag; Game, Onkar; Bhange, Siddheshwar N.; Kumari, Tanya; Ogale, Satishchandra B.; Kurungot, Sreekumar

    2014-08-01

    Here, we report a highly conducting 1-dimensionally (1-D) aligned polyethylenedioxythiophene (PEDOT) along the inner and outer surfaces of a hollow carbon nanofiber (CNF) and its application as a counter electrode in a dye sensitized solar cell (DSSC). The hybrid material (CP-25) displays a conversion efficiency of 7.16% compared to 7.30% for the standard Pt counter electrode, 4.48% for bulk PEDOT and 5.56% for CNF. The enhanced conversion efficiency of CP-25 is attributed to the accomplishment of high conductivity and surface area of PEDOT through the 1-D alignment compared to its bulk counterpart. Reduced charge transfer resistance and high conductivity of CP-25 could be proven by cyclic voltammetry, impedance analysis and Tafel experiments. Further, through a long-term stability test involving efficiency profiling for 20 days, it is observed that CP-25 possesses excellent durability compared to the bulk PEDOT.Here, we report a highly conducting 1-dimensionally (1-D) aligned polyethylenedioxythiophene (PEDOT) along the inner and outer surfaces of a hollow carbon nanofiber (CNF) and its application as a counter electrode in a dye sensitized solar cell (DSSC). The hybrid material (CP-25) displays a conversion efficiency of 7.16% compared to 7.30% for the standard Pt counter electrode, 4.48% for bulk PEDOT and 5.56% for CNF. The enhanced conversion efficiency of CP-25 is attributed to the accomplishment of high conductivity and surface area of PEDOT through the 1-D alignment compared to its bulk counterpart. Reduced charge transfer resistance and high conductivity of CP-25 could be proven by cyclic voltammetry, impedance analysis and Tafel experiments. Further, through a long-term stability test involving efficiency profiling for 20 days, it is observed that CP-25 possesses excellent durability compared to the bulk PEDOT. Electronic supplementary information (ESI) available: Experimental methods and supporting figures. See DOI: 10.1039/c4nr00717d

  4. Carbon nanofiber multiplexed array and Wireless Instantaneous Neurotransmitter Concentration Sensor for simultaneous detection of dissolved oxygen and dopamine

    PubMed Central

    Marsh, Michael P.; Koehne, Jessica E.; Andrews, Russell J.; Meyyappan, M.; Bennet, Kevin E.; Lee, Kendall H.

    2014-01-01

    Purpose While the mechanism of Deep Brain Stimulation (DBS) remains poorly understood, previous studies have shown that it evokes release of neurochemicals and induces activation of functional magnetic resonance imaging (fMRI) blood oxygen level-dependent signal in distinct areas of the brain. Therefore, the main purpose of this paper is to demonstrate the capabilities of the Wireless Instantaneous Neurotransmitter Concentration Sensor system (WINCS) in conjunction with a carbon nanofiber (CNF) multiplexed array electrode as a powerful tool for elucidating the mechanism of DBS through the simultaneous detection of multiple bioactive-molecules. Methods Patterned CNF nanoelectrode arrays were prepared on a 4-inch silicon wafer where each device consists of 3 × 3 electrode pads, 200 μm square, that contain CNFs spaced at 1μm intervals. The multiplexed carbon nanofiber CNF electrodes were integrated with WINCS to detect mixtures of dopamine (DA) and oxygen (O2) using fast scan cyclic voltammetry (FSCV) in vitro. Results First, simultaneous detection of O2 at two spatially different locations, 200 um apart, was demonstrated. Second, simultaneous detection of both O2 and DA at two spatially different locations, using two different decoupled waveforms was demonstrated. Third, controlled studies demonstrated that the waveform must be interleaved to avoid electrode crosstalk artifacts in the acquired data. Conclusions Multiplexed CNF nanoelectrode arrays for electrochemical detection of neurotransmitters show promise for the detection of multiple analytes with the application of time independent decoupled waveforms. Electrochemistry on CNF electrodes may be helpful in elucidating the mechanism of DBS, and may also provide the precision and sensitivity required for future applications in feedback modulated DBS neural control systems. PMID:24688800

  5. Carbon Nanofibers Synthesized on Selective Substrates for Nonvolatile Memory and 3D Electronics

    NASA Technical Reports Server (NTRS)

    Kaul, Anupama B.; Khan, Abdur R.

    2011-01-01

    A plasma-enhanced chemical vapor deposition (PECVD) growth technique has been developed where the choice of starting substrate was found to influence the electrical characteristics of the resulting carbon nanofiber (CNF) tubes. It has been determined that, if the tubes are grown on refractory metallic nitride substrates, then the resulting tubes formed with dc PECVD are also electrically conducting. Individual CNFs were formed by first patterning Ni catalyst islands using ebeam evaporation and liftoff. The CNFs were then synthesized using dc PECVD with C2H2:NH3 = [1:4] at 5 Torr and 700 C, and approximately equal to 200-W plasma power. Tubes were grown directly on degenerately doped silicon <100> substrates with resistivity rho approximately equal to 1-5 meterohm-centimeter, as well as NbTiN. The approximately equal to 200-nanometer thick refractory NbTiN deposited using magnetron sputtering had rho approximately equal to 113 microohm-centimeter and was also chemically compatible with CNF synthesis. The sample was then mounted on a 45 beveled Al holder, and placed inside a SEM (scanning electron microscope). A nanomanipulator probe stage was placed inside the SEM equipped with an electrical feed-through, where tungsten probes were used to make two-terminal electrical measurements with an HP 4156C parameter analyzer. The positive terminal nanoprobe was mechanically manipulated to physically contact an individual CNF grown directly on NbTiN as shown by the SEM image in the inset of figure (a), while the negative terminal was grounded to the substrate. This revealed the tube was electrically conductive, although measureable currents could not be detected until approximately equal to 6 V, after which point current increased sharply until compliance (approximately equal to 50 nA) was reached at approximately equal to 9.5 V. A native oxide on the tungsten probe tips may contribute to a tunnel barrier, which could be the reason for the suppressed transport at low biases

  6. Formation of Bamboo-Like Carbon Nanotubes and Nanofibers Using Co-Si-O and Co-Si Catalysts

    NASA Astrophysics Data System (ADS)

    Chang, Hui Lin; Tzu Kuo, Cheng

    2010-04-01

    Bamboo-like carbon nanotubes were synthesized by microwave plasma chemical vapor deposition (MPCVD) using CH4 and N2 as source gases in various ratios. Two types of catalytic films, namely, a condition 1, Co film/SiO2/Si substrate, and, a Co film/Si substrate layer with rapid thermal annealing (RTA; condition 2), were used as catalysts to grow carbon nanotubes. The interaction between the catalytic film and the Si substrate or between the catalytic film and the SiO2 interlayer occurred during the H2 reduction step before nanotube growth. The chemical compositions of catalytic particles capping the carbon nanotubes were identified by energy-dispersive X-ray spectroscopy (EDS) as Co-Si-O and Co-Si for conditions 1 and 2, respectively. The growth of the base and tip growths was investigated and is suggested to be governed by the capillary effect and the strength of adhesion between the catalytic particles and the underlayer. Transmission electron microscopy (TEM) analysis reveals that the carbon nanotubes and nanofibers have bamboo-like structures with hollow internal compartments. The formation mechanisms of these bamboo-like structures are discussed.

  7. Hierarchical Porous Carbon Materials Derived from Sheep Manure for High-Capacity Supercapacitors.

    PubMed

    Zhang, Caiyun; Zhu, Xiaohong; Cao, Min; Li, Menglin; Li, Na; Lai, Liuqin; Zhu, Jiliang; Wei, Dacheng

    2016-05-10

    3 D capacitance: Hierarchical porous carbon-based electrode materials with a composite structure are prepared from a biomass waste by a facile carbonization and activation process without using any additional templates. Benefiting from the composite structure, the ions experience a variety of environments, which contribute significantly to the excellent electrochemical properties of supercapacitors. PMID:27059168

  8. Characteristics and Electrochemical Performance of Si-Carbon Nanofibers Composite as Anode Material for Binder-Free Lithium Secondary Batteries.

    PubMed

    Hyun, Yura; Park, Heai-Ku; Park, Ho-Seon; Lee, Chang-Seop

    2015-11-01

    The carbon nanofibers (CNFs) and Si-CNFs composite were synthesized using a chemical vapor deposition (CVD) method with an iron-copper catalyst and silicon-covered Ni foam. Acetylene as a carbon source was flowed into the quartz reactor of a tubular furnace heated to 600 degrees C. This temperature was maintained for 10 min to synthesize the CNFs. The morphologies, compositions, and crystal quality of the prepared CNFs were characterized by Scanning electron microscopy (SEM), Energy dispersive spectroscopy (EDS), X-ray Diffraction (XRD), Raman spectroscopy, and X-ray photoelectron spectroscopy (XPS). The electrochemical characteristics of the Si-CNFs composite as an anode of the Li secondary batteries were investigated using a three-electrode cell. The as-deposited Si-CNF composite on the Ni foam was directly employed as an working electrode without any binder, and lithium foil was used as the counter and reference electrode. A glass fiber separator was used as the separator membrane. Two kinds of electrolytes were employed; 1) 1 M LiPF6 was dissolved in a mixture of EC (ethylene carbonate): PC (propylene carbonate): EMC (Ethyl methyl carbonate) in a 1:1:1 volume ratio and 2) 1 M LiClO4 was dissolved in a mixture of propylene carbonate (PC): ethylene carbonate (EC) in a 1:1 volume ratio. The galvanostatic charge-discharge cycling and cyclic voltammetry measurements were carried out at room temperature by using a battery tester. The resulting Si-CNFs composite achieved the large discharge capacity of 613 mAh/g and much improved cycle-ability with the retention rate of 87% after 20 cycles. PMID:26726625

  9. Synthesis of Na-A and/or Na-X zeolite/porous carbon composites from carbonized rice husk

    NASA Astrophysics Data System (ADS)

    Katsuki, Hiroaki; Komarneni, Sridhar

    2009-07-01

    Na-A and/or Na-X zeolite/porous carbon composites were prepared under hydrothermal conditions by NaOH dissolution of silica first from carbonized rice husk followed by addition of NaAlO 2 and in situ crystallization of zeolites i.e., using a two-step process. When a one-step process was used, both Na-A and Na-X zeolites crystallized on the surface of carbon. Na-A or Na-X zeolite crystals were prepared on the porous carbonized rice husk at 90 °C for 2-6 h by changing the SiO 2/Al 2O 3, H 2O/Na 2O and Na 2O/SiO 2 molar ratios of precursors in the two-step process. The surface area and NH 4+-cation exchange capacity (CEC) of Na-A zeolite/porous carbon were found to be 171 m 2/g and 506 meq/100 g, respectively, while those of Na-X zeolite/porous carbon composites were 676 m 2/g and 317 meq/100 g, respectively. Na-A and Na-X zeolites are well-known microporous and hydrophilic materials while carbonized rice husk was found to be mesoporous (pores of ˜3.9 nm) and hydrophobic. These hybrid microporous-mesoporous and hydrophilic-hydrophobic composites are expected to be useful for decontamination of metal cations as well as organic contaminants simultaneously.

  10. Oxygen- and Nitrogen-Enriched 3D Porous Carbon for Supercapacitors of High Volumetric Capacity.

    PubMed

    Li, Jia; Liu, Kang; Gao, Xiang; Yao, Bin; Huo, Kaifu; Cheng, Yongliang; Cheng, Xiaofeng; Chen, Dongchang; Wang, Bo; Sun, Wanmei; Ding, Dong; Liu, Meilin; Huang, Liang

    2015-11-11

    Efficient utilization and broader commercialization of alternative energies (e.g., solar, wind, and geothermal) hinges on the performance and cost of energy storage and conversion systems. For now and in the foreseeable future, the combination of rechargeable batteries and electrochemical capacitors remains the most promising option for many energy storage applications. Porous carbonaceous materials have been widely used as an electrode for batteries and supercapacitors. To date, however, the highest specific capacitance of an electrochemical double layer capacitor is only ∼200 F/g, although a wide variety of synthetic approaches have been explored in creating optimized porous structures. Here, we report our findings in the synthesis of porous carbon through a simple, one-step process: direct carbonization of kelp in an NH3 atmosphere at 700 °C. The resulting oxygen- and nitrogen-enriched carbon has a three-dimensional structure with specific surface area greater than 1000 m(2)/g. When evaluated as an electrode for electrochemical double layer capacitors, the porous carbon structure demonstrated excellent volumetric capacitance (>360 F/cm(3)) with excellent cycling stability. This simple approach to low-cost carbonaceous materials with unique architecture and functionality could be a promising alternative to fabrication of porous carbon structures for many practical applications, including batteries and fuel cells. PMID:26477268

  11. Porous Si spheres encapsulated in carbon shells with enhanced anodic performance in lithium-ion batteries

    SciTech Connect

    Wang, Hui; Wu, Ping Shi, Huimin; Lou, Feijian; Tang, Yawen; Zhou, Tongge; Zhou, Yiming Lu, Tianhong

    2014-07-01

    Highlights: • In situ magnesiothermic reduction route for the formation of porous Si@C spheres. • Unique microstructural characteristics of both porous sphere and carbon matrix. • Enhanced anodic performance in term of cycling stability for lithium-ion batteries. - Abstract: A novel type of porous Si–C micro/nano-hybrids, i.e., porous Si spheres encapsulated in carbon shells (porous Si@C spheres), has been constructed through the pyrolysis of polyvinylidene fluoride (PVDF) and subsequent magnesiothermic reduction methodology by using SiO{sub 2} spheres as precursors. The as-synthesized porous Si@C spheres have been applied as anode materials for lithium-ion batteries (LIBs), and exhibit enhanced anodic performance in term of cycling stability compared with bare Si spheres. For example, the porous Si@C spheres are able to exhibit a high reversible capacity of 900.0 mA h g{sup −1} after 20 cycles at a current density of 0.05 C (1 C = 4200 mA g{sup −1}), which is much higher than that of bare Si spheres (430.7 mA h g{sup −1})

  12. A three-phase homogeneous model for porous electrodes in molten-carbonate fuel cells

    SciTech Connect

    Prins-Jansen, J.A.; Hemmes, K.; Wit, J.H.W. de; Fehribach, J.D.

    1996-05-01

    In this paper a new model for porous electrodes in molten-carbonate fuel cells (MCFC) is presented. The model is based on an averaging technique commonly used in porous-media problems. Important disadvantages of the existing agglomerate model caused by geometric assumptions and restrictions are eliminated in this new model. Unlike the agglomerate model, the new model is suitable for studying three-dimensional and anisotropic problems and incorporating the degree of electrolyte fill. Different reaction mechanisms can easily be incorporated. The validity of the new model is checked and compared with the agglomerate model by fitting the two models to ac-impedance spectra recorded from porous MCFC cathodes.

  13. Nitrogen-Doped Carbon Nanofiber/Molybdenum Disulfide Nanocomposites Derived from Bacterial Cellulose for High-Efficiency Electrocatalytic Hydrogen Evolution Reaction.

    PubMed

    Lai, Feili; Miao, Yue-E; Huang, Yunpeng; Zhang, Youfang; Liu, Tianxi

    2016-02-17

    To remit energy crisis and environmental deterioration, non-noble metal nanocomposites have attracted extensive attention, acting as a fresh kind of cost-effective electrocatalysts for hydrogen evolution reaction (HER). In this work, hierarchically organized nitrogen-doped carbon nanofiber/molybdenum disulfide (pBC-N/MoS2) nanocomposites were successfully prepared via the combination of in situ polymerization, high-temperature carbonization process, and hydrothermal reaction. Attributing to the uniform coating of polyaniline on the surface of bacterial cellulose, the nitrogen-doped carbon nanofiber network acts as an excellent three-dimensional template for hydrothermal growth of MoS2 nanosheets. The obtained hierarchical pBC-N/MoS2 nanocomposites exhibit excellent electrocatalytic activity for HER with small overpotential of 108 mV, high current density of 8.7 mA cm(-2) at η = 200 mV, low Tafel slope of 61 mV dec(-1), and even excellent stability. The greatly improved performance is benefiting from the highly exposed active edge sites of MoS2 nanosheets, the intimate connection between MoS2 nanosheets and the highly conductive nitrogen-doped carbon nanofibers and the three-dimensional networks thus formed. Therefore, this work provides a novel strategy for design and application of bacterial cellulose and MoS2-based nanocomposites as cost-effective HER eletrocatalysts. PMID:26302501

  14. Growth of La{sub 2}CuO{sub 4} nanofibers under a mild condition by using single walled carbon nanotubes as templates

    SciTech Connect

    Gao Lizhen . E-mail: lizhen@mech.uwa.edu.au; Wang Xiaolin; Chua, H.T.; Kawi, Sibudjing

    2006-07-15

    La{sub 2}CuO{sub 4} nanofibers (ca. 30 nm in diameter and 3 {mu}m in length) have been grown in situ by using single walled carbon nanotubes (SWNTs; ca. 2 nm in inner diameter; made via cracking CH{sub 4} over the catalyst of Mg{sub 0.8}Mo{sub 0.05}Ni{sub 0.10}Co{sub 0.05}O {sub x} at 800 deg. C) as templates under mild hydrothermal conditions and a temperature around 60 deg. C. During synthesis, the surfactant poly(ethylene glycol)-block-poly(propylene glycol)-block-poly(ethylene glycol) and H{sub 2}O{sub 2} were added to disperse SWNTs and oxidize the reactants, respectively. The structure of La{sub 2}CuO{sub 4} nanofibers was confirmed by powder X-ray diffraction (XRD) and their morphologies were observed with field emission scanning electron microscope (FESEM) at the hydrothermal synthesis lasting for 5, 20 and 40 h, respectively. The La{sub 2}CuO{sub 4} crystals grew from needle-like (5 h) through stick-like (20 h) and finally to plate-like (40 h) fibers. Twenty hours is an optimum reaction time to obtain regular crystal fibers. The La{sub 2}CuO{sub 4} nanofibers are probably cubic rather than round and may capsulate SWNTs. - Graphical abstract: La{sub 2}CuO{sub 4} nanofibers have been grown in situ by using single walled carbon nanotubes as templates under mild hydrothermal conditions and a temperature around 60 deg. C. The La{sub 2}CuO{sub 4} crystals grew from needle-like (5 h) through stick-like (20 h) and finally to plate-like (40 h) fibers. The La{sub 2}CuO{sub 4} nanofibers are probably cubic rather than round and may capsulate SWNTs.

  15. Carbon nanofibers with radially grown graphene sheets derived from electrospinning for aqueous supercapacitors with high working voltage and energy density.

    PubMed

    Zhao, Lei; Qiu, Yejun; Yu, Jie; Deng, Xianyu; Dai, Chenglong; Bai, Xuedong

    2013-06-01

    Improvement of energy density is an urgent task for developing advanced supercapacitors. In this paper, aqueous supercapacitors with high voltage of 1.8 V and energy density of 29.1 W h kg(-1) were fabricated based on carbon nanofibers (CNFs) and Na2SO4 electrolyte. The CNFs with radially grown graphene sheets (GSs) and small average diameter down to 11 nm were prepared by electrospinning and carbonization in NH3. The radially grown GSs contain between 1 and a few atomic layers with their edges exposed on the surface. The CNFs are doped with nitrogen and oxygen with different concentrations depending on the carbonizing temperature. The supercapacitors exhibit excellent cycling performance with the capacity retention over 93.7% after 5000 charging-discharging cycles. The unique structure, possessing radially grown GSs, small diameter, and heteroatom doping of the CNFs, and application of neutral electrolyte account for the high voltage and energy density of the present supercapacitors. The present supercapacitors are of high promise for practical application due to the high energy density and the advantages of neutral electrolyte including low cost, safety, low corrosivity, and convenient assembly in air. PMID:23624805

  16. Carbon nanofibers with radially grown graphene sheets derived from electrospinning for aqueous supercapacitors with high working voltage and energy density

    NASA Astrophysics Data System (ADS)

    Zhao, Lei; Qiu, Yejun; Yu, Jie; Deng, Xianyu; Dai, Chenglong; Bai, Xuedong

    2013-05-01

    Improvement of energy density is an urgent task for developing advanced supercapacitors. In this paper, aqueous supercapacitors with high voltage of 1.8 V and energy density of 29.1 W h kg-1 were fabricated based on carbon nanofibers (CNFs) and Na2SO4 electrolyte. The CNFs with radially grown graphene sheets (GSs) and small average diameter down to 11 nm were prepared by electrospinning and carbonization in NH3. The radially grown GSs contain between 1 and a few atomic layers with their edges exposed on the surface. The CNFs are doped with nitrogen and oxygen with different concentrations depending on the carbonizing temperature. The supercapacitors exhibit excellent cycling performance with the capacity retention over 93.7% after 5000 charging-discharging cycles. The unique structure, possessing radially grown GSs, small diameter, and heteroatom doping of the CNFs, and application of neutral electrolyte account for the high voltage and energy density of the present supercapacitors. The present supercapacitors are of high promise for practical application due to the high energy density and the advantages of neutral electrolyte including low cost, safety, low corrosivity, and convenient assembly in air.

  17. Carbon Nanofibers Have IgE Adjuvant Capacity but Are Less Potent Than Nanotubes in Promoting Allergic Airway Responses

    PubMed Central

    Samuelsen, Mari; Marioara, Calin Daniel; Løvik, Martinus

    2013-01-01

    There is a growing concern for the possible health impact of nanoparticles. The main objective of this study was to investigate the allergy-promoting capacity of four different carbon nanofiber (CNF) samples in an injection and an airway mouse model of allergy. Secondly, the potency of the CNF was compared to the previously reported allergy-promoting capacity of carbon nanotubes (CNT) in the airway model. Ultrafine carbon black particles (ufCBP) were used as a positive control. Particles were given together with the allergen ovalbumin (OVA) either by subcutaneous injection into the footpad or intranasally to BALB/cA mice. After allergen booster, OVA-specific IgE, IgG1, and IgG2a in serum were measured. In the airway model, inflammation was determined as influx of inflammatory cells (eosinophils, neutrophils, lymphocytes, and macrophages) and by mediators (MCP-1 and TNF-α present in bronchoalveolar fluid (BALF)). CNF and CNT both increased OVA-specific IgE levels in the two models, but in the airway model, the CNT gave a significantly stronger IgE response than the CNF. Furthermore, the CNT and not the CNF promoted eosinophil lung inflammation. Our data therefore suggest that nanotube-associated properties are particularly potent in promoting allergic responses. PMID:24024193

  18. Electrospun Ni-added SnO2-carbon nanofiber composite anode for high-performance lithium-ion batteries.

    PubMed

    Kim, Dongha; Lee, Daehee; Kim, Joosun; Moon, Jooho

    2012-10-24

    The SnO(2) anode is a promising anode for next-generation Li ion batteries because of its high theoretical capacity. However, it exhibits inherent capacity fading because of the large volume change and pulverization that occur during the charge/discharge cycles. The buffer matrix, such as electrospun carbon nanofibers (CNFs), can alleviate this problem to some extent, but SnO(2) particles are thermodynamically incompatible with the carbon matrix such that large Sn agglomerates form after carbonization upon melting of the Sn. Herein, we introduce well-dispersed nanosized SnO(2) attached to CNFs for high-performance anodes developed by Ni presence. The addition of Ni increases the stability of the SnO(2) such that the morphologies of the dispersed SnO(2) phase are modified as a function of the Ni composition. The optimal adding composition is determined to be Ni:Sn = 10:90 wt % in terms of the crystallite size and the distribution uniformity. A high capacity retention of 447.6 mA h g(-1) after 100 cycles can be obtained for 10 wt % Ni-added SnO(2)-CNFs, whereas Ni-free Sn/SnO(2)-CNFs have a capacity retention of 304.6 mA h g(-1). PMID:22999049

  19. Airbrushed nickel nanoparticles for large-area growth of vertically aligned carbon nanofibers on metal (Al, Cu, Ti) surfaces.

    PubMed

    Sarac, Mehmet F; Anderson, Bryan D; Pearce, Ryan C; Railsback, Justin G; Oni, Adedapo A; White, Ryan M; Hensley, Dale K; LeBeau, James M; Melechko, Anatoli V; Tracy, Joseph B

    2013-09-25

    Vertically aligned carbon nanofibers (VACNFs) were grown by plasma-enhanced chemical vapor deposition (PECVD) using Ni nanoparticle (NP) catalysts that were deposited by airbrushing onto Si, Al, Cu, and Ti substrates. Airbrushing is a simple method for depositing catalyst NPs over large areas that is compatible with roll-to-roll processing. The distribution and morphology of VACNFs are affected by the airbrushing parameters and the composition of the metal foil. Highly concentrated Ni NPs in heptane give more uniform distributions than pentane and hexanes, resulting in more uniform coverage of VACNFs. For VACNF growth on metal foils, Si micropowder was added as a precursor for Si-enriched coatings formed in situ on the VACNFs that impart mechanical rigidity. Interactions between the catalyst NPs and the metal substrates impart control over the VACNF morphology. Growth of carbon nanostructures on Cu is particularly noteworthy because the miscibility of Ni with Cu poses challenges for VACNF growth, and carbon nanostructures anchored to Cu substrates are desired as anode materials for Li-ion batteries and for thermal interface materials. PMID:24016419

  20. Converting biowaste corncob residue into high value added porous carbon for supercapacitor electrodes.

    PubMed

    Qu, Wen-Hui; Xu, Yuan-Yuan; Lu, An-Hui; Zhang, Xiang-Qian; Li, Wen-Cui

    2015-08-01

    In this report, corncob residue, the main by-product in the furfural industry, is used as a precursor to prepare porous carbon by a simple and direct thermal treatment: one-step activation without pre-carbonization. As a consequence, the corncob residue derived porous carbon achieves a high surface area of 1210 m(2) g(-1) after ash-removal. The carbon material has the advantages of low cost and low environmental impact, with a superior electrochemical performance compared to those polymer-based synthetic carbons as electrode material for a supercapacitor. The carbon electrode exhibits a high capacitance of 314 F g(-1) in 6M KOH electrolyte. The corresponding sample also shows a superb cycling stability. Almost no capacitance decay was observed after 100,000 cycles. The excellent electrochemical performance is due to the combination of a high specific surface area with a fraction of mesopores and highly stable structure. PMID:25898091

  1. Enhanced CO2/N2 Selectivity in Amidoxime-Modified Porous Carbon

    SciTech Connect

    Mahurin, Shannon Mark; Gorka, Joanna; Nelson, Kimberly M; Mayes, Richard T; Dai, Sheng

    2014-01-01

    In this work, we examine the use of the amidoxime functional group grafted onto a hierarchical porous carbon framework for the selective capture and removal of carbon dioxide from combustion streams. Measured CO2/N2 ideal selectivity values for the amidoxime-grafted carbon were significantly higher than the pristine porous carbon with improvements of 65%. Though the overall CO2 capacity decreased slightly for the activated carbon from 4.97 mmol g-1 to 4.24 mmol g-1 after surface modification due to a reduction in the total surface area, the isosteric heats of adsorption increased after amidoxime incorporation indicating an increased interaction of CO2 with the sorbent. Total capacity was reproducible and stable after multiple adsorption/desorption cycles with no loss of capacity suggesting that modification with the amidoxime group is a potential method to enhance carbon capture.

  2. Effects of potassium on Ni-K/Al2O3 catalysts in the synthesis of carbon nanofibers by catalytic hydrogenation of CO2.

    PubMed

    Chen, Ching S; Lin, Jarrn H; You, Jiann H; Yang, Kuo H

    2010-03-25

    Commercially available Ni/Al(2)O(3) samples containing various concentrations of potassium were used to achieve carbon deposition from CO(2) via catalytic hydrogenation. Experimental results show that K additives can induce the formation of carbon nanofibers or carbon deposition on Ni/Al(2)O(3) during the reverse water-gas shift reaction. This work proposes that the formation rate of carbon deposition depends closely on ensemble control, suggesting that the ensemble size necessary to form carbon may be approximately 0.5 potassium atoms. The results of CO(2) temperature-programmed desorption provide strong evidence that the new adsorption sites for CO(2) created on Ni-K/Al(2)O(3) closely depend upon the synthesis of carbon nanofibers. It is found that some potassium-related active phases obtained by calcination and reduction pretreatments can participate in the carbon deposition reaction. The formation pathway for carbon deposition suggests that the main source of carbon deposition is CO(2) and that the pathway is independent of the reaction products CO and CH(4) in the reverse water-gas shift reaction. PMID:19655780

  3. Size and Promoter Effects on Stability of Carbon-Nanofiber-Supported Iron-Based Fischer–Tropsch Catalysts

    PubMed Central

    2016-01-01

    The Fischer–Tropsch Synthesis converts synthesis gas from alternative carbon resources, including natural gas, coal, and biomass, to hydrocarbons used as fuels or chemicals. In particular, iron-based catalysts at elevated temperatures favor the selective production of C2–C4 olefins, which are important building blocks for the chemical industry. Bulk iron catalysts (with promoters) were conventionally used, but these deactivate due to either phase transformation or carbon deposition resulting in disintegration of the catalyst particles. For supported iron catalysts, iron particle growth may result in loss of catalytic activity over time. In this work, the effects of promoters and particle size on the stability of supported iron nanoparticles (initial sizes of 3–9 nm) were investigated at industrially relevant conditions (340 °C, 20 bar, H2/CO = 1). Upon addition of sodium and sulfur promoters to iron nanoparticles supported on carbon nanofibers, initial catalytic activities were high, but substantial deactivation was observed over a period of 100 h. In situ Mössbauer spectroscopy revealed that after 20 h time-on-stream, promoted catalysts attained 100% carbidization, whereas for unpromoted catalysts, this was around 25%. In situ carbon deposition studies were carried out using a tapered element oscillating microbalance (TEOM). No carbon laydown was detected for the unpromoted catalysts, whereas for promoted catalysts, carbon deposition occurred mainly over the first 4 h and thus did not play a pivotal role in deactivation over 100 h. Instead, the loss of catalytic activity coincided with the increase in Fe particle size to 20–50 nm, thereby supporting the proposal that the loss of active Fe surface area was the main cause of deactivation. PMID:27330847

  4. Drug loading into porous calcium carbonate microparticles by solvent evaporation.

    PubMed

    Preisig, Daniel; Haid, David; Varum, Felipe J O; Bravo, Roberto; Alles, Rainer; Huwyler, Jörg; Puchkov, Maxim

    2014-08-01

    Drug loading into porous carriers may improve drug release of poorly water-soluble drugs. However, the widely used impregnation method based on adsorption lacks reproducibility and efficiency for certain compounds. The aim of this study was to evaluate a drug-loading method based on solvent evaporation and crystallization, and to investigate the underlying drug-loading mechanisms. Functionalized calcium carbonate (FCC) microparticles and four drugs with different solubility and permeability properties were selected as model substances to investigate drug loading. Ibuprofen, nifedipine, losartan potassium, and metronidazole benzoate were dissolved in acetone or methanol. After dispersion of FCC, the solvent was removed under reduced pressure. For each model drug, a series of drug loads were produced ranging from 25% to 50% (w/w) in steps of 5% (w/w). Loading efficiency was qualitatively analyzed by scanning electron microscopy (SEM) using the presence of agglomerates and drug crystals as indicators of poor loading efficiency. The particles were further characterized by mercury porosimetry, specific surface area measurements, differential scanning calorimetry, and USP2 dissolution. Drug concentration was determined by HPLC. FCC-drug mixtures containing equivalent drug fractions but without specific loading strategy served as reference samples. SEM analysis revealed high efficiency of pore filling up to a drug load of 40% (w/w). Above this, agglomerates and separate crystals were significantly increased, indicating that the maximum capacity of drug loading was reached. Intraparticle porosity and specific surface area were decreased after drug loading because of pore filling and crystallization on the pore surface. HPLC quantification of drugs taken up by FCC showed only minor drug loss. Dissolution rate of FCC loaded with metronidazole benzoate and nifedipine was faster than the corresponding FCC-drug mixtures, mainly due to surface enlargement, because only small

  5. A novel nonenzymatic sensor based on CuO nanoneedle/graphene/carbon nanofiber modified electrode for probing glucose in saliva.

    PubMed

    Ye, Daixin; Liang, Guohai; Li, Huixiang; Luo, Juan; Zhang, Song; Chen, Hui; Kong, Jilie

    2013-11-15

    Here, we report on a novel nonenzymatic amperometric glucose sensor based on CuO nanoneedle/graphene/carbon nanofiber modified electrode. The results of the scanning electron microscopy indicate that electronic network was formed through their direct binding with the graphene/carbon nanofiber, which leads to larger active surface areas and faster electron transfer for the glucose sensor. High electrocatalytic activity toward the oxidation of glucose was observed with a rapid response (<2 s), a low detection limit (0.1 µM), a wide and useful linear range (1-5.3 mM) as well as good stability and repeatability. Moreover, the common interfering species, such as ascorbic acid, uric acid, dopamine and so forth did not cause obvious interference. The sensor can also be used for quantification of glucose concentration in real saliva samples. Therefore, this work has demonstrated a simple and effective sensing platform for nonenzymatic detection of glucose. PMID:24148397

  6. Engineered magnetic core-shell SiO2/Fe microspheres and "medusa-like" microspheres of SiO2/iron oxide/carbon nanofibers or nanotubes.

    PubMed

    Mero, On; Sougrati, Moulay-Tahar; Jumas, Jean-Claude; Margel, Shlomo

    2014-08-19

    Iron oxide (IO) thin coatings of controlled thickness on SiO2 microspheres of narrow size distribution were prepared by decomposition at 160 °C of triiron dodecacarbonyl onto silica microspheres dispersed in diethylene glycol diethyl ether free of surfactant or stabilizer. The dried washed SiO2/IO core-shell microspheres were annealed at different temperatures and time periods under inert (Ar) or reducing (H2) atmosphere. The effect of temperature on the chemical composition, morphology, crystallinity, and magnetic properties of the IO and the elemental Fe nanoparticles type coatings onto the SiO2 core microspheres has been elucidated. "Medusa-like" SiO2/IO/carbon nanofibers and tubes particles were prepared by CVD of ethylene on the surface of the SiO2/IO microspheres at different temperatures. The morphology change of the grafted carbon nanofibers and tubes as a function of the CVD temperature was also elucidated. PMID:25089849

  7. Bulk and Surface Chemistry Modification of Highly Porous Carbon for Supercapacitors

    NASA Astrophysics Data System (ADS)

    Candelaria, Stephanie L.

    Highly porous carbon prepared through sol-gel processing is an excellent electrode material for supercapacitors, also known as electrochemical capacitors, because of its high surface area and pore volume, good conductivity, and low cost. Research has mostly focused on increasing the surface area of the carbon to improve charge storage, but there are limits to how large this value can be while still maintaining good electrochemical performance of the material. Alternatively, carbon can be modified with foreign elements, either in the bulk or on the pore surfaces, to induce pseudocapacitive reactions that can increase capacitance. Modified samples can also be tested at higher working voltages, which significantly increase the energy and power densities. In this work, highly porous carbon is modified with nitrogen and tested as electrodes in supercapacitors. Modification significantly increases the wettability of the carbon, and the capacitance increases with increasing nitrogen added. However, too much nitrogen can cause pore blockage and decrease accessible surface area, limiting the capacitance. Highly porous carbon, both with and without nitrogen on the pore surfaces, is then tested at higher working voltages. Increasing the voltage from 2V to 3V significantly improves both the energy density and power density. Finally, porous carbon was also synthesized from lignin, a complex polymer derived from natural resources and a waste product in the paper industry. Purification removed over half of the impurities and resulted in porous carbon with four times the internal surface area compared to unpurified lignin. When tested in devices, lignin-derived carbon shows promise as low-cost, renewable material for high performance supercapacitors.

  8. Facile Carbonization of Microporous Organic Polymers into Hierarchically Porous Carbons Targeted for Effective CO2 Uptake at Low Pressures.

    PubMed

    Gu, Shuai; He, Jianqiao; Zhu, Yunlong; Wang, Zhiqiang; Chen, Dongyang; Yu, Guipeng; Pan, Chunyue; Guan, Jianguo; Tao, Kai

    2016-07-20

    The advent of microporous organic polymers (MOPs) has delivered great potential in gas storage and separation (CCS). However, the presence of only micropores in these polymers often imposes diffusion limitations, which has resulted in the low utilization of MOPs in CCS. Herein, facile chemical activation of the single microporous organic polymers (MOPs) resulted in a series of hierarchically porous carbons with hierarchically meso-microporous structures and high CO2 uptake capacities at low pressures. The MOPs precursors (termed as MOP-7-10) with a simple narrow micropore structure obtained in this work possess moderate apparent BET surface areas ranging from 479 to 819 m(2) g(-1). By comparing different activating agents for the carbonization of these MOPs matrials, we found the optimized carbon matrials MOPs-C activated by KOH show unique hierarchically porous structures with a significant expansion of dominant pore size from micropores to mesopores, whereas their microporosity is also significantly improved, which was evidenced by a significant increase in the micropore volume (from 0.27 to 0.68 cm(3) g(-1)). This maybe related to the collapse and the structural rearrangement of the polymer farmeworks resulted from the activation of the activating agent KOH at high temperature. The as-made hierarchically porous carbons MOPs-C show an obvious increase in the BET surface area (from 819 to 1824 m(2) g(-1)). And the unique hierarchically porous structures of MOPs-C significantly contributed to the enhancement of the CO2 capture capacities, which are up to 214 mg g(-1) (at 273 K and 1 bar) and 52 mg g(-1) (at 273 K and 0.15 bar), superior to those of the most known MOPs and porous carbons. The high physicochemical stabilities and appropriate isosteric adsorption heats as well as high CO2/N2 ideal selectivities endow these hierarchically porous carbon materials great potential in gas sorption and separation. PMID:27332739

  9. Synthesis of porous sulfonated carbon as a potential adsorbent for phenol wastewater.

    PubMed

    Prabhu, Azhagapillai; Al Shoaibi, Ahmed; Srinivasakannan, C

    2015-01-01

    The work reports a facile synthesis procedure for preparation of porous sulfonated carbons and its suitability for adsorption of phenol. The sulfonated carbon was synthesized utilizing a simplified, single-step, shorter duration process by sulfonation, dehydration and carbonization of sucrose in sulfuric acid and tetraethylorthosilicate. The surface and internal structures of the adsorbents were characterized utilizing various characterization techniques to understand the porous nature and surface functional groups of the porous matrix. Adsorption capacity was found to be highest for the sample heat treated at 600 °C, with the maximum adsorption capacity of 440 mg/g at 30 °C. The adsorption isotherms were tested with the Freundlich and Langmuir adsorption isotherms models to identify the appropriate adsorption mechanism. PMID:26524451

  10. Depressing the hydrogenation and decomposition reaction in H2O2 synthesis by supporting AuPD on oxygen functionalized carbon nanofibers

    SciTech Connect

    Villa, Alberto; Freakley, Simon J.; Schiavoni, Marco; Edwards, Jennifer K.; Hammond, Ceri; Wang, Wu; Wang, Di; Prati, Laura; Dimitratos, Nikolaos; Hutchings, Graham J.; Veith, Gabriel M.

    2015-12-03

    In this work, we show that the introduction of acidic oxygen functionalities to the surface of carbon nanofibers serves to depress the hydrogenation and the decomposition of hydrogen peroxide during the direct synthesis of H2O2. Furthermore, the presence of acidic groups enhances the H2O2 productivity in the case of supported AuPd nanoparticles.

  11. Preparation and electrochemical performance of hyper-networked Li4Ti5O12/carbon hybrid nanofiber sheets for a battery-supercapacitor hybrid system

    NASA Astrophysics Data System (ADS)

    Choi, Hong Soo; Kim, TaeHoon; Im, Ji Hyuk; Park, Chong Rae

    2011-10-01

    Hyper-networked Li4Ti5O12/carbon hybrid nanofiber sheets that contain both a faradaically rechargeable battery-type component, namely Li4Ti5O12, and a non-faradaically rechargeable supercapacitor-type component, namely N-enriched carbon, are prepared by electrospinning and their dual function as a negative electrode of lithium-ion batteries (LIBs) and a capacitor is tested for a new class of hybrid energy storage (denoted BatCap). An aqueous solution composed of polyvinylpyrrolidone, lithium hydroxide, titanium(IV) bis(ammonium-lactato)dihydroxide and ammonium persulfate is electrospun to obtain hyper-networked nanofiber sheets. Next, the sheets are exposed to pyrrole monomer vapor to prepare the polypyrrole-coated nanofiber sheets (PPy-HNS). The hyper-networked Li4Ti5O12/N-enriched carbon hybrid nanofiber sheets (LTO/C-HNS) are then obtained by a stepwise heat treatment of the PPy-HNS. The LTO/C-HNS deliver a specific capacity of 135 mAh g - 1 at 4000 mA g - 1 as a negative electrode for LIBs. In addition, potentiodynamic experiments are performed using a full cell with activated carbon (AC) as the positive electrode and LTO/C-HNS as the negative electrode to estimate the capacitance properties. This new asymmetric electrode system exhibits a high energy density of 91 W kg - 1 and 22 W kg - 1 at power densities of 50 W kg - 1 and 4000 W kg - 1, respectively, which are superior to the values observed for the {AC} \\parallel {AC} symmetric electrode system.

  12. Ultrahigh methanol electro-oxidation activity of PtRu nanoparticles prepared on TiO2-embedded carbon nanofiber support

    NASA Astrophysics Data System (ADS)

    Ito, Yudai; Takeuchi, Taizo; Tsujiguchi, Takuya; Abdelkareem, Mohammad Ali; Nakagawa, Nobuyoshi

    2013-11-01

    A TiO2-embedded carbon nanofiber (TECNF) was proposed as a promising support of the PtRu nanocatalyst for the methanol oxidation reaction. The nanofiber support was prepared by the electrospinning of polyacrylonitrile (PAN) with TiO2 nanoparticles followed by carbonization and steam activation of the nanofiber, and lastly, the PtRu nanoparticles deposition. Cyclic voltammetry (CV) revealed a significantly high MOR activity for the PtRu/TECNF compared to that of the PtRu nanoparticles deposited on different supports, i.e., carbon black (C), TiO2 nanoparticles (TiO2), a mixture of these nanoparticles (C + TiO2) and carbon nanofiber (CNF). The MOR activity was high in the order of PtRu/TECNF > PtRu/CNF > PtRu/(C + TiO2) > PtRu/C >> PtRu/TiO2. The activity of PtRu/TECNF increased with an increase in the weight ratio of Ti/C for TECNF up to 1.0 and then decreased. The MOR mass activity of PtRu/TECNF at the optimum Ti/C ratio was 4 times higher than that of PtRu/C. The ultrahigh catalytic activity of PtRu/TECNF is attributed to the metal-support interaction, which efficiently occurs at the PtRu/TECNF structure. The ultrahigh catalytic activity was also confirmed by the two-times higher DMFC power output using PtRu/TECNF, in spite of quarter the PtRu loading on the electrode, compared to that using the commercial PtRu/C.

  13. Synthesis of Na-A and/or Na-X zeolite/porous carbon composites from carbonized rice husk

    SciTech Connect

    Katsuki, Hiroaki; Komarneni, Sridhar

    2009-07-15

    Na-A and/or Na-X zeolite/porous carbon composites were prepared under hydrothermal conditions by NaOH dissolution of silica first from carbonized rice husk followed by addition of NaAlO{sub 2} and in situ crystallization of zeolites i.e., using a two-step process. When a one-step process was used, both Na-A and Na-X zeolites crystallized on the surface of carbon. Na-A or Na-X zeolite crystals were prepared on the porous carbonized rice husk at 90 deg. C for 2-6 h by changing the SiO{sub 2}/Al{sub 2}O{sub 3}, H{sub 2}O/Na{sub 2}O and Na{sub 2}O/SiO{sub 2} molar ratios of precursors in the two-step process. The surface area and NH{sub 4}{sup +}-cation exchange capacity (CEC) of Na-A zeolite/porous carbon were found to be 171 m{sup 2}/g and 506 meq/100 g, respectively, while those of Na-X zeolite/porous carbon composites were 676 m{sup 2}/g and 317 meq/100 g, respectively. Na-A and Na-X zeolites are well-known microporous and hydrophilic materials while carbonized rice husk was found to be mesoporous (pores of {approx}3.9 nm) and hydrophobic. These hybrid microporous-mesoporous and hydrophilic-hydrophobic composites are expected to be useful for decontamination of metal cations as well as organic contaminants simultaneously. - Graphical Abstract: Novel Na-X zeolite/porous carbon composite.

  14. Preparation of porous carbons from polymeric precursors modified with acrylated kraft lignin

    NASA Astrophysics Data System (ADS)

    Sobiesiak, M.

    2016-04-01

    The presented studies concern the preparation of porous carbons from a BPA.DA-St polymer containing acrylated kraft lignin as a monomer. The porous polymeric precursor in the form of microspheres was synthesized in suspension polymerization process. Next samples of the polymer were impregnated with acetic acid or aqueous solution of acetates (potassium or ammonia), dried and carbonised in nitrogen atmosphere at 450°C. After carbonization microspherical shape of the materials was remained, that is desired feature for potential application in chromatography or SPE technique. Chemical and textural properties of the porous carbon adsorbents were characterized using infrared spectroscopy (ATR-FTIR), thermogravimetry analyses with mass spectrometry of released gases (TG-MS) and nitrogen sorption experiments. The presented studies revealed the impregnation is useful method for development of porous structure of carbonaceous materials. The highest values of porous structure parameters were obtained when acetic acid and ammonium acetate were used as impregnating substances. On the surface of the materials oxygen functional groups are present that is important for specific interactions during sorption processes. The highest contents of functionalities were observed for carbon BPA.DA-St-LA-C-AcNH4.

  15. Preparation and characterization of ordered porous carbons for increasing hydrogen storage behaviors

    SciTech Connect

    Lee, Seul-Yi; Park, Soo-Jin

    2011-10-15

    We prepared ordered porous carbons (PCs) by using a replication method that had well-organized mesoporous silica as a template with various carbonization temperatures in order to investigate the possibility of energy storage materials. The microstructure and morphologies of the samples are characterized by XRD, TEM, and FT-Raman spectroscopy. N{sub 2} adsorption isotherms are analyzed by the t-plot method, as well as the BET and the H-K method in order to characterize the specific surface area, pore volume, and pore size distribution of the samples, respectively. The capacity of the hydrogen adsorption of the samples is evaluated by BEL-HP at 77 K and 1 bar. From the results, we are able to confirm that the synthesis of the samples can be accurately governed by the carbonization temperature, which is one of the effective parameters for developing the textural properties of the carbon materials, which affects the behaviors of the hydrogen storage. - Graphical abstract: It is described that the considerable long-range ordering and the presence of mono-dimensional aligned channels between the two aligned nanorods of the porous framework from the SBA-15 was retained in the T-950 sample during the carbonization process. Highlights: > Ordered porous carbons (PCs) are synthesized with various carbonization temperatures by using a replication method. > Carbonization temperature plays an important role in shrinking the micropores during the carbonization process of PCs. > The textural and structural properties of the PCs are good parameters for enhancing the hydrogen storage capacity.

  16. On the use of mesophase pitch for the preparation of hierarchical porous carbon monoliths by nanocasting

    NASA Astrophysics Data System (ADS)

    Adelhelm, Philipp; Cabrera, Karin; Smarsly, Bernd M.

    2012-02-01

    A detailed study is given on the synthesis of a hierarchical porous carbon, possessing both meso- and macropores, using a mesophase pitch (MP) as the carbon precursor. This carbon material is prepared by the nanocasting approach involving the replication of a porous silica monolith (hard templating). While this carbon material has already been tested in energy storage applications, various detailed aspects of its formation and structure are addressed in this study. Scanning electron microscopy (SEM), Hg porosimetry and N2 physisorption are used to characterize the morphology and porosity of the carbon replica. A novel approach for the detailed analysis of wide-angle x-ray scattering (WAXS) from non-graphitic carbons is applied to quantitatively compare the graphene microstructures of carbons prepared using MP and furfuryl alcohol (FA). This WAXS analysis underlines the importance of the carbon precursor in the synthesis of templated porous carbon materials via the nanocasting route. Our study demonstrates that a mesophase pitch is a superior precursor whenever a high-purity, low-micropore-content and well-developed graphene structure is desired.

  17. Porous electrolyte retainer for molten carbonate fuel cell

    DOEpatents

    Singh, Raj N.; Dusek, Joseph T.

    1983-06-21

    A porous tile for retaining molten electrolyte within a fuel cell is prepared by sintering particles of lithium aluminate into a stable structure. The tile is assembled between two porous metal plates which serve as electrodes with fuels gases such as H.sub.2 and CO opposite to oxidant gases such as O.sub.2 and CO.sub.2. The tile is prepared with a porosity of 55-65% and a pore size distribution selected to permit release of sufficient molten electrolyte to wet but not to flood the adjacent electrodes.

  18. Porous electrolyte retainer for molten carbonate fuel cell. [lithium aluminate

    DOEpatents

    Singh, R.N.; Dusek, J.T.

    1979-12-27

    A porous tile for retaining molten electrolyte within a fuel cell is prepared by sintering particles of lithium aluminate into a stable structure. The tile is assembled between two porous metal plates which serve as electrodes with fuels gases such as H/sub 2/ and CO opposite to oxidant gases such as O/sub 2/ and CO/sub 2/. The tile is prepared with a porosity of 55 to 65% and a pore size distribution selected to permit release of sufficient molten electrolyte to wet but not to flood the adjacent electrodes.

  19. Occupational Exposure Assessment in Carbon Nanotube and Nanofiber Primary and Secondary Manufacturers: Mobile Direct-Reading Sampling

    PubMed Central

    DAHM, MATTHEW M.; EVANS, DOUGLAS E.; SCHUBAUER-BERIGAN, MARY K.; BIRCH, M. EILEEN; DEDDENS, JAMES A.

    2015-01-01

    Research Significance Toxicological evidence suggests the potential for a wide range of health effects from exposure to carbon nanotubes (CNTs) and carbon nanofibers (CNFs). To date, there has been much focus on the use of direct-reading instruments (DRIs) to assess multiple airborne exposure metrics for potential exposures to CNTs and CNFs due to their ease of use and ability to provide instantaneous results. Still, uncertainty exists in the usefulness and interpretation of the data. To address this gap, air-monitoring was conducted at six sites identified as CNT and CNF manufacturers or users and results were compared with filter-based metrics. Methods Particle number, respirable mass, and active surface area concentrations were monitored with a condensation particle counter, a photometer, and a diffusion charger, respectively. The instruments were placed on a mobile cart and used as area monitors in parallel with filter-based elemental carbon (EC) and electron microscopy samples. Repeat samples were collected on consecutive days, when possible, during the same processes. All instruments in this study are portable and routinely used for industrial hygiene sampling. Results Differences were not observed among the various sampled processes compared with concurrent indoor or outdoor background samples while examining the different DRI exposure metrics. Such data were also inconsistent with results for filter-based samples collected concurrently at the same sites [Dahm MM, Evans DE, Schubauer-Berigan MK et al. (2012) Occupational exposure assessment in CNT and nanofiber primary and secondary manufacturers. Ann Occup Hyg; 56: 542–56]. Significant variability was seen between these processes as well as the indoor and outdoor backgrounds. However, no clear pattern emerged linking the DRI results to the EC or the microscopy data (CNT and CNF structure counts). Conclusions Overall, no consistent trends were seen among similar processes at the various sites. The DRI

  20. Rod-shape porous carbon derived from aniline modified lignin for symmetric supercapacitors

    NASA Astrophysics Data System (ADS)

    Wang, Keliang; Cao, Yuhe; Wang, Xiaomin; Castro, Maria Andrea; Luo, Bing; Gu, Zhengrong; Liu, Jun; Hoefelmeyer, James D.; Fan, Qihua

    2016-03-01

    Rod-shape porous carbon was prepared from aniline modified lignin via KOH activation and used as electrode materials for supercapacitors. The specific surface area, pore size and shape could be modulated by the carbonization temperature, which significantly affected the electrochemical performance. Unique rod-shape carbon with massive pores and a high BET surface area of 2265 m2 g-1 were obtained at 700 °C in contrast to irregular morphology created at other carbonization temperatures. In 6 mol L-1 KOH electrolyte, a specific capacitance of 336 F g-1, small resistance of 0.9 Ω and stable charge/discharge at current density of 1 A g-1 after 1, 000 cycles were achieved using rod-shape porous carbon as electrodes in an electrical double layer capacitor.

  1. Condiment-Derived 3D Architecture Porous Carbon for Electrochemical Supercapacitors.

    PubMed

    Qian, Wenjing; Zhu, Jingyue; Zhang, Ye; Wu, Xiao; Yan, Feng

    2015-10-01

    The one-step synthesis of porous carbon nanoflakes possessing a 3D texture is achieved by cooking (carbonization) a mixture containing two condiments, sodium glutamate (SG) and sodium chloride, which are commonly used in kitchens. The prepared 3D porous carbons are composed of interconnected carbon nanoflakes and possess instinct heteroatom doping such as nitrogen and oxygen, which furnishes the electrochemical activity. The combination of micropores and mesopores with 3D configurations facilitates persistent and fast ion transport and shorten diffusion pathways for high-performance supercapacitor applications. Sodium glutamate carbonized at 800 °C exhibits high charge storage capacity with a specific capacitance of 320 F g(-1) in 6 m KOH at a current density of 1 A g(-1) and good stability over 10,000 cycles. PMID:26150228

  2. Carbon Microfibers with Hierarchical Porous Structure from Electrospun Fiber-Like Natural Biopolymer

    PubMed Central

    Liang, Yeru; Wu, Dingcai; Fu, Ruowen

    2013-01-01

    Electrospinning offers a powerful route for building one-dimensional (1D) micro/nanostructures, but a common requirement for toxic or corrosive organic solvents during the preparation of precursor solution has limited their large scale synthesis and broad applications. Here we report a facile and low-cost way to prepare 1D porous carbon microfibers by using an electrospun fiber-like natural product, i.e., silk cocoon, as precursor. We surprisingly found that by utilizing a simple carbonization treatment, the cocoon microfiber can be directly transformed into 1D carbon microfiber of ca. 6 μm diameter with a unique three-dimensional porous network structure composed of interconnected carbon nanoparticles of 10~40 nm diameter. We further showed that the as-prepared carbon product presents superior electrochemical performance as binder-free electrodes of supercapacitors and good adsorption property toward organic vapor. PMID:23350027

  3. Use of ceramic porous membranes in molten carbonate fuel cells

    SciTech Connect

    Passalacqua, E.; Freni, S.; Patti, A.; Maggio, G.

    1996-12-31

    The diffusion of alkali vapours in the anode compartment of a DIR-MCFC produces the deactivation of the internal reforming catalyst. Sets of ceramic porous membranes purposed to limit the diffusion have been manufactured by different techniques and the influence of the preparation technique and of the preparative variables on the morphological characteristics of the membranes structures has been studied.

  4. Highly porous activated carbons prepared from carbon rich Mongolian anthracite by direct NaOH activation

    NASA Astrophysics Data System (ADS)

    Byamba-Ochir, Narandalai; Shim, Wang Geun; Balathanigaimani, M. S.; Moon, Hee

    2016-08-01

    Highly porous activated carbons (ACs) were prepared from Mongolian raw anthracite (MRA) using sodium hydroxide as an activation agent by varying the mass ratio (powdered MRA/NaOH) as well as the mixing method of chemical agent and powdered MRA. The specific BET surface area and total pore volume of the prepared MRA-based activated carbons (MACs) are in the range of 816-2063 m2/g and of 0.55-1.61 cm3/g, respectively. The pore size distribution of MACs show that most of the pores are in the range from large micropores to small mesopores and their distribution can be controlled by the mass ratio and mixing method of the activating agent. As expected from the intrinsic property of the MRA, the highly graphitic surface morphology of prepared carbons was confirmed from Raman spectra and transmission electron microscopy (TEM) studies. Furthermore the FTIR and XPS results reveal that the preparation of MACs with hydrophobic in nature is highly possible by controlling the mixing conditions of activating agent and powdered MRA. Based on all the results, it is suggested that the prepared MACs could be used for many specific applications, requiring high surface area, optimal pore size distribution, proper surface hydrophobicity as well as strong physical strength.

  5. Activation of micropore-confined sulfur within hierarchical porous carbon for lithium-sulfur batteries

    NASA Astrophysics Data System (ADS)

    Kim, Jung-Joon; Kim, Hee Soo; Ahn, Jihoon; Lee, Kyung Jae; Yoo, Won Cheol; Sung, Yung-Eun

    2016-02-01

    Hierarchical porous carbon is often used in Li-S batteries due to the widely perceived benefits regarding the wide range of pore sizes. However, such notions are based solely on demonstrations of improved cyclic performances, and specific evidence to prove the utilization of the pores is yet to be found. Herein, we report, for the first time, the evidence for gradual activation of micropore-confined sulfur within porous carbon structures. By systematic comparison of microporous and hierarchical porous structures, we show that at sufficiently low current, sulfur infused hierarchical porous structures display a slowly activated and reversible reaction at 1.75 V vs Li/Li+ during discharge. This is in addition to the conventionally reported two voltage plateau at 2.3 and 2.1 V. Furthermore, the effects of LiNO3 decomposition on the system and the electrochemical mechanism behind the activation process is elucidated. Overall, the findings supplement the currently known electrochemical mechanisms occurring within porous structures and pave the way for more efficient utilization of hierarchical porous structures for applications in Li-S batteries.

  6. A novel strategy to synthesize hierarchical, porous carbohydrate-derived carbon with tunable properties.

    PubMed

    Wang, Shiping; Liu, Ruihan; Han, Chuanlong; Wang, Jing; Li, Mingming; Yao, Jia; Li, Haoran; Wang, Yong

    2014-11-21

    Hydrothermal carbonization (HTC) of carbohydrate is an interesting candidate for the preparation of carbon materials, as it provides an easy, inexpensive and environmental friendly route. However, it is difficult to prepare porous carbon materials by a straight HTC process. Herein, the solubilising technology of micelles was introduced to direct the HTC of fructose by using an amphiphilic block copolymer, poly-(4-vinylpyridine)-block-poly-(ethylene glycol) (P4VP-PEG), as a structure-directing agent. By this strategy, hierarchical porous carbon materials with tunable properties were prepared. It was found that P4VP-PEG micelles could solubilize fructose and confine the formation of primary carbon domains during a sol-gel process. And the micelle size could be adjusted easily by changing the preparation conditions. Accordingly, the particle size of the obtained carbon materials was effectively tuned from 20 to 100 nm by the direction of the primary micelle size. After calcination, the hierarchical porous carbon materials were evidenced as effective electrode materials for supercapacitor with a capacitance of ∼197 F at 1 A g(-1), which was almost four times higher than the carbon materials prepared by a straight HTC process. PMID:25267462

  7. Highly porous activated carbons from resource-recovered Leucaena leucocephala wood as capacitive deionization electrodes.

    PubMed

    Hou, Chia-Hung; Liu, Nei-Ling; Hsi, Hsing-Cheng

    2015-12-01

    Highly porous activated carbons were resource-recovered from Leucaena leucocephala (Lam.) de Wit. wood through combined chemical and physical activation (i.e., KOH etching followed by CO2 activation). This invasive species, which has severely damaged the ecological economics of Taiwan, was used as the precursor for producing high-quality carbonaceous electrodes for capacitive deionization (CDI). Carbonization and activation conditions strongly influenced the structure of chars and activated carbons. The total surface area and pore volume of activated carbons increased with increasing KOH/char ratio and activation time. Overgasification induced a substantial amount of mesopores in the activated carbons. In addition, the electrochemical properties and CDI electrosorptive performance of the activated carbons were evaluated; cyclic voltammetry and galvanostatic charge/discharge measurements revealed a typical capacitive behavior and electrical double layer formation, confirming ion electrosorption in the porous structure. The activated-carbon electrode, which possessed high surface area and both mesopores and micropores, exhibited improved capacitor characteristics and high electrosorptive performance. Highly porous activated carbons derived from waste L. leucocephala were demonstrated to be suitable CDI electrode materials. PMID:26135977

  8. Reduction of charge and discharge polarization by cobalt nanoparticles-embedded carbon nanofibers for Li-O2 batteries.

    PubMed

    Kim, Yun-Jung; Lee, Hongkyung; Lee, Dong Jin; Park, Jung-Ki; Kim, Hee-Tak

    2015-08-10

    The problem of high charge polarization is one of the most significant challenges in current nonaqueous Li-O2 batteries. The development of an electrode for the oxygen evolution reaction (OER) at reduced overpotential is thus essential. Here, we suggest a binder-free electrode based on Co nanoparticles embedded in carbon nanofibers (Co-CNFs), which simultaneously reduces the charge and discharge polarization and extends cycling stability. Co-CNF gives rise to a lower discharge polarization because of an enhanced oxygen reduction reaction activity compared to Co-free CNF. Although the embedment of Co does not enhance the OER activity, it significantly reduces charge overvoltage by forming easily decomposable amorphous Li2 O2 . A mechanism for the formation of amorphous Li2 O2 is suggested in terms of charge localization induced by the Co NPs. The findings suggest a new electrode design strategy of combining inexpensive metals and carbon materials for modulating the phase of the discharge product. PMID:26178625

  9. Controllable growth of Prussian blue nanostructures on carboxylic group-functionalized carbon nanofibers and its application for glucose biosensing.

    PubMed

    Wang, Li; Ye, Yinjian; Zhu, Haozhi; Song, Yonghai; He, Shuijian; Xu, Fugang; Hou, Haoqing

    2012-11-16

    Glucose detection is very important in biological analysis, clinical diagnosis and the food industry, and especially for the routine monitoring of diabetes. This work presents an electrochemical approach to the detection of glucose based on Prussian blue (PB) nanostructures/carboxylic group-functionalized carbon nanofiber (FCNF) nanocomposites. The hybrid nanocomposites were constructed by growing PB onto the FCNFs. The obtained PB-FCNF nanocomposites were characterized by scanning electron microscopy, x-ray diffraction and x-ray photoelectron spectroscopy. The mechanism of formation of PB-FCNF nanocomposites was investigated and is discussed in detail. The PB-FCNF modified glassy carbon electrode (PB-FCNF/GCE) shows good electrocatalysis toward the reduction of H(2)O(2), a product from the reduction of O(2) followed by glucose oxidase (GOD) catalysis of the oxidation of glucose to gluconic acid. Further immobilizing GOD on the PB-FCNF/GCE, an amperometric glucose biosensor was achieved by monitoring the generated H(2)O(2) under a relatively negative potential. The resulting glucose biosensor exhibited a rapid response of 5 s, a low detection limit of 0.5 μM, a wide linear range of 0.02-12 mM, a high sensitivity of 35.94 μA cm(-2) mM(-1), as well as good stability, repeatability and selectivity. The sensor might be promising for practical application. PMID:23090569

  10. Fabrication of graphene sheets intercalated with manganese oxide/carbon nanofibers: toward high-capacity energy storage.

    PubMed

    Kwon, Oh Seok; Kim, Taejoon; Lee, Jun Seop; Park, Seon Joo; Park, Hyun-Woo; Kang, Minjeong; Lee, Ji Eun; Jang, Jyongsik; Yoon, Hyeonseok

    2013-01-28

    Herein, 3D nanohybrid architectures consisting of MnO(x) nanocrystals, carbon nanofibers (CNFs), and graphene sheets are fabricated. MnO(x) -decorated CNFs (MCNFs) with diameters of about 50 nm are readily obtained via single-nozzle co-electrospinning, followed by heat treatment. The MCNFs are then intercalated between graphene sheets, yielding the ternary nanohybrid MCNF/reduced graphene oxide (RGO). This straightforward synthesis process readily affords product on a scale of tens of grams. The ultrathin CNFs, which might be a promising alternative to carbon nanotubes (CNTs), overcome the low electrical conductivity of the excellent pseudocapacitive component, MnO(x) . Furthermore, the graphene sheets separated by the MCNFs boost the electrochemical performance of the nanohybrid electrodes. These nanohybrid electrodes exhibit enhanced specific capacitances compared with a sheet electrode fabricated of MCNF-only or RGO-only. Evidently, the RGO sheet acts as a conductive channel inside the nanohybrid, while the intercalated MCNFs increase the efficiency of the ion and charge transfer in the nanohybrid. The proposed nanohybrid architectures are expected to lay the foundation for the design and fabrication of high-performance electrodes. PMID:23034820

  11. Amorphous flower-like molybdenum-sulfide-@-nitrogen-doped-carbon-nanofiber film for use in the hydrogen-evolution reaction.

    PubMed

    Zhang, Xiaoyan; Li, Libo; Guo, Yaxiao; Liu, Dong; You, Tianyan

    2016-06-15

    A novel amorphous flower-like molybdenum sulfides@nitrogen doped carbon nanofibers (MoSx@NCNFs) films are successfully synthesized by combining electrospinning, carbonization and a mild hydrothermal process. NCNFs, as a conductive substrate, can accelerate the electron transfer rate and depress the aggregation of MoSx nanoparticles. The resultant amorphous flower-like MoSx on NCNFs exposes abundant S(2-)/S2(2-) active edge sites which is of great importance for hydrogen evolution reaction (HER) catalytic performance. Electrochemical measurements demonstrate the superior electrocatalytic activity of MoSx@NCNFs toward HER deriving from the synergistic effect between NCNFs and amorphous MoSx. The overpotential is only 137 mV to reach the current density of 10 mA cm(-2) with a Tafel slope of 41 mV decade(-1) at MoSx@NCNFs. Meanwhile, MoSx@NCNFs exhibits satisfactory long-time stability for HER. Noteworthy, the obtained composites show a free-standing structure which can be directly used as electrode materials. This work provides a feasible way to design promising noble-metal free electrocatalysts in the aspect of energy conversion. PMID:27015391

  12. Au@Ag nanorods based electrochemical immunoassay for immunoglobulin G with signal enhancement using carbon nanofibers-polyamidoamine dendrimer nanocomposite.

    PubMed

    Ma, Lina; Ning, Danlei; Zhang, Hongfang; Zheng, Jianbin

    2015-06-15

    Au@Ag nanorods (Au@AgNRs) was utilized to construct a novel sandwich-type electrochemical immunosensor for the detection of immunoglobulin G (IgG). The sensor was prepared by immoblizing capture antibodies on the amine-terminated nanocomposite of carbon nanofibers-polyamidoamine dendrimer (CNFs-PAMAM), whilst the trace tag was prepared by loading anti-human IgG on Au@AgNRs. The "built-in" Ag layer on Au nanorods was characterized by UV-vis extinction spectra, transmission electron microscopy and energy dispersive spectroscopy. The results of cyclic voltammetry indicated that modifying CNFs-PAMAM nanocomposite on glassy carbon electrode enabled 177 times of peak current increase of Ag in the bimetallic nanorods. The peak current was quantitatively related with the concentration of the target protein IgG via the formation of immunocomplex. After the parameter optimization, the oxidative peak current of silver was proportional to the concentration of IgG in a wide linear range of six orders of magnitude with a low detection limit of 0.5 fg mL(-1). Besides, this sensor showed acceptable reproducibility and stability, and thus the strategy reported here has great promise for extension to the other disease biomarkers. PMID:25569874

  13. Cell response to single-walled carbon nanotubes in hybrid porous collagen sponges.

    PubMed

    Mao, Hongli; Kawazoe, Naoki; Chen, Guoping

    2015-02-01

    Three-dimensional (3D) porous collagen sponges incorporated with single-walled carbon nanotubes (SWCNTs) were prepared and used for 3D culture of bovine articular chondrocytes (BACs). The pore structures of the sponges were controlled by using ice particulates as a porogen material. The responses of cells to SWCNTs were investigated in this 3D cell culture system by evaluation of cell functions and cellular uptake of SWCNTs. The results showed that cells adhered and spatially distributed in the porous sponges. The incorporation of SWCNTs in the porous sponges promoted cell proliferation and production of sulfated glycosaminoglycans (sGAG). Confocal Raman imaging revealed that SWCNTs could be internalized by cells. The hybrid porous sponges not only provided nanostructured pore surfaces to facilitate cell proliferation and extracellular matrix (ECM) secretion but also supplied nanomaterials for cellular uptake which may be useful for biomedical applications. PMID:25543985

  14. Synthesis of sulfonated porous carbon nanospheres solid acid by a facile chemical activation route

    SciTech Connect

    Chang, Binbin Guo, Yanzhen; Yin, Hang; Zhang, Shouren; Yang, Baocheng

    2015-01-15

    Generally, porous carbon nanospheres materials are usually prepared via a template method, which is a multi-steps and high-cost strategy. Here, we reported a porous carbon nanosphere solid acid with high surface area and superior porosity, as well as uniform nanospheical morphology, which prepared by a facile chemical activation with ZnCl{sub 2} using resorcinol-formaldehyde (RF) resins spheres as precursor. The activation of RF resins spheres by ZnCl{sub 2} at 400 °C brought high surface area and large volume, and simultaneously retained numerous oxygen-containing and hydrogen-containing groups due to the relatively low processing temperature. The presence of these functional groups is favorable for the modification of –SO{sub 3}H groups by a followed sulfonation treating with sulphuric acid and organic sulfonic acid. The results of N{sub 2} adsorption–desorption and electron microscopy clearly showed the preservation of porous structure and nanospherical morphology. Infrared spectra certified the variation of surface functional groups after activation and the successful modification of –SO{sub 3}H groups after sulfonation. The acidities of catalysts were estimated by an indirect titration method and the modified amount of –SO{sub 3}H groups were examined by energy dispersive spectra. The results suggested sulfonated porous carbon nanospheres catalysts possessed high acidities and –SO{sub 3}H densities, which endowed their significantly catalytic activities for biodiesel production. Furthermore, their excellent stability and recycling property were also demonstrated by five consecutive cycles. - Graphical abstract: Sulfonated porous carbon nanospheres with high surface area and superior catalytic performance were prepared by a facile chemical activation route. - Highlights: • Porous carbon spheres solid acid prepared by a facile chemical activation. • It owns high surface area, superior porosity and uniform spherical morphology. • It possesses

  15. A Sinter-Resistant Catalytic System Based on Platinum Nanoparticles Supported on TiO2 Nanofibers and Covered by Porous Silica

    SciTech Connect

    Dai, Yunqian; Lim, Byungkwon; Yang, Yong; Cobley, Claire M.; Li, Weiyang; Cho, Eun Chul; Grayson, Benjamin; Fanson, Paul T.; Campbell, Charles T.; Sun, Yueming; Xia, Younan

    2010-10-25

    Platinum is a key catalyst that is invaluable in many important industrial processes such as CO oxidation in catalytic converters, oxidation and reduction reactions in fuel cells, nitric acid production, and petroleum cracking.[1] Many of these applications utilize Pt nanoparticles supported on oxides or porous carbon.[2] However, in practical applications that involve high temperatures (typically higher than 3008C), the Pt nanoparticles tend to lose their specific surface area and thus catalytic activity during operation because of sintering. Recent studies have shown that a porous oxide shell can act as a physical barrier to prevent sintering of unsupported metal nanoparticles and, at the same time, provide channels for chemical species to reach the surface of the nanoparticles, thus allowing the catalytic reaction to occur. This concept has been demonstrated in several systems, including Pt@SiO2,[3] Pt@CoO,[4] Pt/CeO2@SiO2,[5] Pd@SiO2,[6] Au@SiO2,[7] Au@SnO2 [8] and Au@ZrO2 [9] core– shell nanostructures. Despite these results, a sinter-resistant system has not been realized in supported Pt nanoparticle catalysts.

  16. Hierarchical Electrospun and Cooperatively Assembled Nanoporous Ni/NiO/MnOx/Carbon Nanofiber Composites for Lithium Ion Battery Anodes.

    PubMed

    Bhaway, Sarang M; Chen, Yu-Ming; Guo, Yuanhao; Tangvijitsakul, Pattarasai; Soucek, Mark D; Cakmak, Miko; Zhu, Yu; Vogt, Bryan D

    2016-08-01

    A facile method to fabricate hierarchically structured fiber composites is described based on the electrospinning of a dope containing nickel and manganese nitrate salts, citric acid, phenolic resin, and an amphiphilic block copolymer. Carbonization of these fiber mats at 800 °C generates metallic Ni-encapsulated NiO/MnOx/carbon composite fibers with average BET surface area (150 m(2)/g) almost 3 times higher than those reported for nonporous metal oxide nanofibers. The average diameter (∼900 nm) of these fiber composites is nearly invariant of chemical composition and can be easily tuned by the dope concentration and electrospinning conditions. The metallic Ni nanoparticle encapsulation of NiO/MnOx/C fibers leads to enhanced electrical conductivity of the fibers, while the block copolymers template an internal nanoporous morphology and the carbon in these composite fibers helps to accommodate volumetric changes during charging. These attributes can lead to lithium ion battery anodes with decent rate performance and long-term cycle stability, but performance strongly depends on the composition of the composite fibers. The composite fibers produced from a dope where the metal nitrate is 66% Ni generates the anode that exhibits the highest reversible specific capacity at high rate for any composition, even when including the mass of the nonactive carbon and Ni(0) in the calculation of the capacity. On the basis of the active oxides alone, near-theoretical capacity and excellent cycling stability are achieved for this composition. These cooperatively assembled hierarchical composites provide a platform for fundamentally assessing compositional dependencies for electrochemical performance. Moreover, this electrospinning strategy is readily scalable for the fabrication of a wide variety of nanoporous transition metal oxide fibers. PMID:27399605

  17. Nitrogen-Doped Carbon Nanoparticle-Carbon Nanofiber Composite as an Efficient Metal-Free Cathode Catalyst for Oxygen Reduction Reaction.

    PubMed

    Panomsuwan, Gasidit; Saito, Nagahiro; Ishizaki, Takahiro

    2016-03-23

    Metal-free nitrogen-doped carbon materials are currently considered at the forefront of potential alternative cathode catalysts for the oxygen reduction reaction (ORR) in fuel cell technology. Despite numerous efforts in this area over the past decade, rational design and development of a new catalyst system based on nitrogen-doped carbon materials via an innovative approach still present intriguing challenges in ORR catalysis research. Herein, a new kind of nitrogen-doped carbon nanoparticle-carbon nanofiber (NCNP-CNF) composite with highly efficient and stable ORR catalytic activity has been developed via a new approach assisted by a solution plasma process. The integration of NCNPs and CNFs by the solution plasma process can lead to a unique morphological feature and modify physicochemical properties. The NCNP-CNF composite exhibits a significantly enhanced ORR activity through a dominant four-electron pathway in an alkaline solution. The enhancement in ORR activity of NCNP-CNF composite can be attributed to the synergistic effects of good electron transport from highly graphitized CNFs as well as abundance of exposed catalytic sites and meso/macroporosity from NCNPs. More importantly, NCNP-CNF composite reveals excellent long-term durability and high tolerance to methanol crossover compared with those of a commercial 20 wt % supported on Vulcan XC-72. We expect that NCNP-CNF composite prepared by this synthetic approach can be a promising metal-free cathode catalyst candidate for ORR in fuel cells and metal-air batteries. PMID:26908214

  18. Electrospun Nanofibers for Neural and Tissue Engineering

    NASA Astrophysics Data System (ADS)

    Xia, Younan

    2009-03-01

    Electrospinning has been exploited for almost one century to process polymers and other materials into nanofibers with controllable compositions, diameters, porosities, and porous structures for a variety of applications. Owing to its small size, high porosity, and large surface area, a nonwoven mat of electrospun nanofibers can serve as an ideal scaffold to mimic the extra cellular matrix for cell attachment and nutrient transportation. The nanofiber itself can also be functionalized through encapsulation or attachment of bioactive species such as extracellular matrix proteins, enzymes, and growth factors. In addition, the nanofibers can be further assembled into a variety of arrays or architectures by manipulating their alignment, stacking, or folding. All these attributes make electrospinning a powerful tool for generating nanostructured materials for a range of biomedical applications that include controlled release, drug delivery, and tissue engineering. This talk will focus on the use of electrospun nanofibers as scaffolds for neural and bone tissue engineering.

  19. Cobalt monoxide-doped porous graphitic carbon microspheres for supercapacitor application

    PubMed Central

    Yang, Zheng-Chun; Tang, Chun-Hua; Zhang, Yu; Gong, Hao; Li, Xu; Wang, John

    2013-01-01

    A novel design and facile synthesis process for carbon based hybrid materials, i.e., cobalt monoxide (CoO)-doped graphitic porous carbon microspheres (Co-GPCMs), have been developed. With the synthesis strategy, the mixture of cobalt gluconate, α-cyclodextrin and poly (ethylene oxide)106-poly (propylene oxide)70-poly (ethylene oxide)106 is treated hydrothermally, followed by pyrolysis in argon. The resultant Co-GPCMs exhibits a porous carbon matrix with localized graphitic structure while CoO nanodots are embedded in the carbon frame. Thus, the Co-GPCMs effectively combine the electric double-layer capacitance and pseudo-capacitance when used as the electrode in supercapacitor, which lead to a higher operation voltage (1.6 V) and give rise to a significantly higher energy density. This study provides a new research strategy for electrode materials in high energy density supercapacitors. PMID:24113335

  20. Nanofibers Comprising Yolk-Shell Sn@void@SnO/SnO₂ and Hollow SnO/SnO₂ and SnO₂ Nanospheres via the Kirkendall Diffusion Effect and Their Electrochemical Properties.

    PubMed

    Cho, Jung Sang; Kang, Yun Chan

    2015-09-01

    Nanofibers with a unique structure comprising Sn@void@SnO/SnO2 yolk-shell nanospheres and hollow SnO/SnO2 and SnO2 nanospheres are prepared by applying the nanoscale Kirkendall diffusion process in conventional electrospinning process. Under a reducing atmosphere, post-treatment of tin 2-ethylhexanoate-polyvinylpyrrolidone electrospun nanofibers produce carbon nanofibers with embedded spherical Sn nanopowders. The Sn nanopowders are linearly aligned along the carbon nanofiber axis without aggregation of the nanopowders. Under an air atmosphere, oxidation of the Sn-C composite nanofibers produce nanofibers comprising Sn@void@SnO/SnO2 yolk-shell nanospheres and hollow SnO/SnO2 and SnO2 nanospheres, depending on the post-treatment temperature. The mean sizes of the hollow nanospheres embedded within tin oxide nanofibers post-treated at 500 °C and 600 °C are 146 and 117 nm, respectively. For the 250th cycle, the discharge capacities of the nanofibers prepared by the nanoscale Kirkendall diffusion process post-treated at 400 °C, 500 °C, and 600 °C at a high current density of 2 A g(-1) are 663, 630, and 567 mA h g(-1), respectively. The corresponding capacity retentions are 77%, 84%, and 78%, as calculated from the second cycle. The nanofibers prepared by applying the nanoscale Kirkendall diffusion process exhibit superior electrochemical properties compared with those of the porous-structured SnO2 nanofibers prepared by the conventional post-treatment process. PMID:26058833